{"id":12802,"date":"2025-09-23T06:47:21","date_gmt":"2025-09-23T05:47:21","guid":{"rendered":"https:\/\/mcqsadda.com\/?p=12802"},"modified":"2025-10-22T10:33:59","modified_gmt":"2025-10-22T09:33:59","slug":"hydrocarbons-top-100-mcqs-with-answer-and-explanation","status":"publish","type":"post","link":"https:\/\/mcqsadda.com\/index.php\/2025\/09\/23\/hydrocarbons-top-100-mcqs-with-answer-and-explanation\/","title":{"rendered":"Hydrocarbons Top 100 MCQs With Answer and Explanation"},"content":{"rendered":"\n<p class=\"has-large-font-size\"><strong><mark style=\"background-color:rgba(0, 0, 0, 0)\" class=\"has-inline-color has-luminous-vivid-orange-color\">1. Hydrocarbons are compounds made up of:<\/mark><\/strong><br>a) Carbon and oxygen<br>b) Carbon and hydrogen<br>c) Carbon and nitrogen<br>d) Carbon and sulphur<br><strong>Answer:<\/strong> b) Carbon and hydrogen<br><strong>Explanation:<\/strong> Hydrocarbons are organic compounds consisting only of carbon and hydrogen atoms.<\/p>\n\n\n\n<p class=\"has-large-font-size\"><strong><mark style=\"background-color:rgba(0, 0, 0, 0)\" class=\"has-inline-color has-luminous-vivid-orange-color\">2. The simplest hydrocarbon is:<br><\/mark><\/strong>a) Methane<br>b) Ethane<br>c) Propane<br>d) Acetylene<br><strong>Answer:<\/strong> a) Methane<br><strong>Explanation:<\/strong> Methane (CH\u2084) is the first member of alkanes.<\/p>\n\n\n\n<p class=\"has-large-font-size\"><strong><mark style=\"background-color:rgba(0, 0, 0, 0)\" class=\"has-inline-color has-luminous-vivid-orange-color\">3. Alkanes are also called:<br><\/mark><\/strong>a) Olefins<br>b) Paraffins<br>c) Aromatics<br>d) Acetylenes<br><strong>Answer:<\/strong> b) Paraffins<br><strong>Explanation:<\/strong> Alkanes are saturated hydrocarbons (CnH\u2082n+2), also called paraffins (little reactivity).<\/p>\n\n\n\n<p class=\"has-large-font-size\"><strong><mark style=\"background-color:rgba(0, 0, 0, 0)\" class=\"has-inline-color has-luminous-vivid-orange-color\">4. General formula of alkanes is:<br><\/mark><\/strong>a) CnH\u2082n<br>b) CnH\u2082n+2<br>c) CnH\u2082n\u20132<br>d) CnH\u2082n+1<br><strong>Answer:<\/strong> b) CnH\u2082n+2<br><strong>Explanation:<\/strong> Alkanes follow general formula CnH\u2082n+2.<\/p>\n\n\n\n<p class=\"has-large-font-size\"><strong><mark style=\"background-color:rgba(0, 0, 0, 0)\" class=\"has-inline-color has-luminous-vivid-orange-color\">5. Ethane (C\u2082H\u2086) belongs to:<br><\/mark><\/strong>a) Alkanes<br>b) Alkenes<br>c) Alkynes<br>d) Aromatics<br><strong>Answer:<\/strong> a) Alkanes<br><strong>Explanation:<\/strong> Ethane is a saturated hydrocarbon with single bonds only.<\/p>\n\n\n\n<p class=\"has-large-font-size\"><strong><mark style=\"background-color:rgba(0, 0, 0, 0)\" class=\"has-inline-color has-luminous-vivid-orange-color\">6. Which alkane has 3 carbon atoms?<br><\/mark><\/strong>a) Methane<br>b) Ethane<br>c) Propane<br>d) Butane<br><strong>Answer:<\/strong> c) Propane<br><strong>Explanation:<\/strong> Propane (C\u2083H\u2088) is the third member of alkanes.<\/p>\n\n\n\n<p class=\"has-large-font-size\"><strong><mark style=\"background-color:rgba(0, 0, 0, 0)\" class=\"has-inline-color has-luminous-vivid-orange-color\">7. Butane is used in:<br><\/mark><\/strong>a) Fertilizer industry<br>b) LPG as cooking fuel<br>c) Explosives<br>d) Plastics<br><strong>Answer:<\/strong> b) LPG as cooking fuel<br><strong>Explanation:<\/strong> LPG is mainly a mixture of propane and butane.<\/p>\n\n\n\n<p class=\"has-large-font-size\"><strong><mark style=\"background-color:rgba(0, 0, 0, 0)\" class=\"has-inline-color has-luminous-vivid-orange-color\">8. Isomerism starts from which alkane?<br><\/mark><\/strong>a) Methane<br>b) Ethane<br>c) Propane<br>d) Butane<br><strong>Answer:<\/strong> d) Butane<br><strong>Explanation:<\/strong> Butane (C\u2084H\u2081\u2080) has two isomers \u2013 n-butane and isobutane.<\/p>\n\n\n\n<p class=\"has-large-font-size\"><strong><mark style=\"background-color:rgba(0, 0, 0, 0)\" class=\"has-inline-color has-luminous-vivid-orange-color\">9. Cycloalkanes have general formula:<br><\/mark><\/strong>a) CnH\u2082n+2<br>b) CnH\u2082n<br>c) CnH\u2082n\u20132<br>d) CnH\u2082n+1<br><strong>Answer:<\/strong> b) CnH\u2082n<br><strong>Explanation:<\/strong> Cycloalkanes are ring hydrocarbons with general formula CnH\u2082n.<\/p>\n\n\n\n<p class=\"has-large-font-size\"><strong><mark style=\"background-color:rgba(0, 0, 0, 0)\" class=\"has-inline-color has-luminous-vivid-orange-color\">10. The IUPAC name of isobutane is:<br><\/mark><\/strong>a) 2-methylpropane<br>b) 2-methylbutane<br>c) 3-methylpentane<br>d) 2,2-dimethylpropane<br><strong>Answer:<\/strong> a) 2-methylpropane<br><strong>Explanation:<\/strong> Isobutane is a branched-chain isomer of butane.<\/p>\n\n\n\n<p class=\"has-large-font-size\"><strong><mark style=\"background-color:rgba(0, 0, 0, 0)\" class=\"has-inline-color has-luminous-vivid-orange-color\">11. Alkanes are generally obtained from:<br><\/mark><\/strong>a) Natural gas and petroleum<br>b) Coal<br>c) Air<br>d) Plants only<br><strong>Answer:<\/strong> a) Natural gas and petroleum<br><strong>Explanation:<\/strong> Natural gas contains methane, ethane, propane, and butane.<\/p>\n\n\n\n<p class=\"has-large-font-size\"><strong><mark style=\"background-color:rgba(0, 0, 0, 0)\" class=\"has-inline-color has-luminous-vivid-orange-color\">12. The main constituent of natural gas is:<br><\/mark><\/strong>a) Ethane<br>b) Methane<br>c) Propane<br>d) Butane<br><strong>Answer:<\/strong> b) Methane<br><strong>Explanation:<\/strong> Natural gas has ~80\u201390% methane.<\/p>\n\n\n\n<p class=\"has-large-font-size\"><strong><mark style=\"background-color:rgba(0, 0, 0, 0)\" class=\"has-inline-color has-luminous-vivid-orange-color\">13. Which alkane is also known as marsh gas?<br><\/mark><\/strong>a) Ethane<br>b) Propane<br>c) Methane<br>d) Butane<br><strong>Answer:<\/strong> c) Methane<br><strong>Explanation:<\/strong> Methane forms in marshes by decomposition of organic matter.<\/p>\n\n\n\n<p class=\"has-large-font-size\"><strong><mark style=\"background-color:rgba(0, 0, 0, 0)\" class=\"has-inline-color has-luminous-vivid-orange-color\">14. Which alkane is used as a refrigerant in the form of liquefied gas?<br><\/mark><\/strong>a) Methane<br>b) Ethane<br>c) Propane<br>d) Butane<br><strong>Answer:<\/strong> c) Propane<br><strong>Explanation:<\/strong> Propane is used in refrigeration and air-conditioning systems.<\/p>\n\n\n\n<p class=\"has-large-font-size\"><strong><mark style=\"background-color:rgba(0, 0, 0, 0)\" class=\"has-inline-color has-luminous-vivid-orange-color\">15. Combustion of alkanes produces:<br><\/mark><\/strong>a) CO only<br>b) CO\u2082 + H\u2082O<br>c) H\u2082 only<br>d) CO\u2082 + N\u2082<br><strong>Answer:<\/strong> b) CO\u2082 + H\u2082O<br><strong>Explanation:<\/strong> Complete combustion of alkanes \u2192 carbon dioxide + water.<\/p>\n\n\n\n<p class=\"has-large-font-size\"><strong><mark style=\"background-color:rgba(0, 0, 0, 0)\" class=\"has-inline-color has-luminous-vivid-orange-color\">16. Incomplete combustion of alkanes produces:<br><\/mark><\/strong>a) Only CO\u2082<br>b) Carbon monoxide and soot<br>c) Methanol<br>d) Oxygen<br><strong>Answer:<\/strong> b) Carbon monoxide and soot<br><strong>Explanation:<\/strong> Limited oxygen supply \u2192 CO + C (soot).<\/p>\n\n\n\n<p class=\"has-large-font-size\"><strong><mark style=\"background-color:rgba(0, 0, 0, 0)\" class=\"has-inline-color has-luminous-vivid-orange-color\">17. The reaction of alkanes with chlorine in presence of sunlight is called:<br><\/mark><\/strong>a) Addition reaction<br>b) Substitution reaction<br>c) Oxidation reaction<br>d) Hydrogenation<br><strong>Answer:<\/strong> b) Substitution reaction<br><strong>Explanation:<\/strong> Alkanes undergo free radical substitution with halogens.<\/p>\n\n\n\n<p class=\"has-large-font-size\"><strong><mark style=\"background-color:rgba(0, 0, 0, 0)\" class=\"has-inline-color has-luminous-vivid-orange-color\">18. The main reaction of alkanes is:<br><\/mark><\/strong>a) Addition<br>b) Substitution<br>c) Polymerization<br>d) Oxidation<br><strong>Answer:<\/strong> b) Substitution<br><strong>Explanation:<\/strong> Alkanes are saturated \u2192 undergo substitution.<\/p>\n\n\n\n<p class=\"has-large-font-size\"><strong><mark style=\"background-color:rgba(0, 0, 0, 0)\" class=\"has-inline-color has-luminous-vivid-orange-color\">19. Pyrolysis of alkanes is:<br><\/mark><\/strong>a) Heating in presence of oxygen<br>b) Heating in absence of air<br>c) Reaction with halogens<br>d) Oxidation<br><strong>Answer:<\/strong> b) Heating in absence of air<br><strong>Explanation:<\/strong> Pyrolysis = thermal decomposition \u2192 smaller alkanes + alkenes.<\/p>\n\n\n\n<p class=\"has-large-font-size\"><strong><mark style=\"background-color:rgba(0, 0, 0, 0)\" class=\"has-inline-color has-luminous-vivid-orange-color\">20. The process of converting alkanes into aromatic hydrocarbons is:<br><\/mark><\/strong>a) Hydrogenation<br>b) Aromatization<br>c) Isomerization<br>d) Substitution<br><strong>Answer:<\/strong> b) Aromatization<br><strong>Explanation:<\/strong> Aromatization converts alkanes into benzene\/toluene (catalysts used).<\/p>\n\n\n\n<p class=\"has-large-font-size\"><strong><mark style=\"background-color:rgba(0, 0, 0, 0)\" class=\"has-inline-color has-luminous-vivid-orange-color\">21. The octane number of a fuel indicates:<br><\/mark><\/strong>a) Density<br>b) Antiknocking property<br>c) Calorific value<br>d) Cost<br><strong>Answer:<\/strong> b) Antiknocking property<br><strong>Explanation:<\/strong> Higher octane number = better fuel efficiency.<\/p>\n\n\n\n<p class=\"has-large-font-size\"><strong><mark style=\"background-color:rgba(0, 0, 0, 0)\" class=\"has-inline-color has-luminous-vivid-orange-color\">22. Iso-octane is used as:<br><\/mark><\/strong>a) Reference fuel in octane number scale<br>b) Solvent<br>c) Explosive<br>d) Refrigerant<br><strong>Answer:<\/strong> a) Reference fuel in octane number scale<br><strong>Explanation:<\/strong> Iso-octane = 100 octane rating, reference standard.<\/p>\n\n\n\n<p class=\"has-large-font-size\"><strong><mark style=\"background-color:rgba(0, 0, 0, 0)\" class=\"has-inline-color has-luminous-vivid-orange-color\">23. Knocking in petrol engines is reduced by adding:<br><\/mark><\/strong>a) Lead tetraethyl<br>b) Alcohol<br>c) Acetone<br>d) Hydrogen<br><strong>Answer:<\/strong> a) Lead tetraethyl<br><strong>Explanation:<\/strong> Lead tetraethyl (historically) improved octane rating.<\/p>\n\n\n\n<p class=\"has-large-font-size\"><strong><mark style=\"background-color:rgba(0, 0, 0, 0)\" class=\"has-inline-color has-luminous-vivid-orange-color\">24. Which alkane is used in the production of carbon black?<br><\/mark><\/strong>a) Methane<br>b) Ethane<br>c) Acetylene<br>d) Natural gas<br><strong>Answer:<\/strong> d) Natural gas<br><strong>Explanation:<\/strong> Methane-rich natural gas is burnt in limited oxygen \u2192 carbon black (tyres, inks).<\/p>\n\n\n\n<p class=\"has-large-font-size\"><strong><mark style=\"background-color:rgba(0, 0, 0, 0)\" class=\"has-inline-color has-luminous-vivid-orange-color\">25. Higher alkanes are generally found in:<br><\/mark><\/strong>a) Natural gas<br>b) Kerosene and diesel fractions of petroleum<br>c) Coal gas<br>d) Air<br><strong>Answer:<\/strong> b) Kerosene and diesel fractions of petroleum<br><strong>Explanation:<\/strong> Higher alkanes (C\u2081\u2080\u2013C\u2081\u2086) are in kerosene, diesel, and lubricating oils.<\/p>\n\n\n\n<p class=\"has-large-font-size\"><strong><mark style=\"background-color:rgba(0, 0, 0, 0)\" class=\"has-inline-color has-luminous-vivid-orange-color\">26. Alkenes are also called:<br><\/mark><\/strong>a) Paraffins<br>b) Olefins<br>c) Aromatics<br>d) Acetylenes<br><strong>Answer:<\/strong> b) Olefins<br><strong>Explanation:<\/strong> Alkenes (CnH\u2082n) are unsaturated hydrocarbons with double bonds, called olefins.<\/p>\n\n\n\n<p class=\"has-large-font-size\"><strong><mark style=\"background-color:rgba(0, 0, 0, 0)\" class=\"has-inline-color has-luminous-vivid-orange-color\">27. General formula of alkenes is:<br><\/mark><\/strong>a) CnH\u2082n+2<br>b) CnH\u2082n<br>c) CnH\u2082n\u20132<br>d) CnH\u2082n\u20131<br><strong>Answer:<\/strong> b) CnH\u2082n<br><strong>Explanation:<\/strong> Alkenes have one double bond, general formula CnH\u2082n.<\/p>\n\n\n\n<p class=\"has-large-font-size\"><strong><mark style=\"background-color:rgba(0, 0, 0, 0)\" class=\"has-inline-color has-luminous-vivid-orange-color\">28. The first member of alkenes is:<br><\/mark><\/strong>a) Methene<br>b) Ethene<br>c) Propene<br>d) Butene<br><strong>Answer:<\/strong> b) Ethene<br><strong>Explanation:<\/strong> Ethene (C\u2082H\u2084) is the simplest alkene.<\/p>\n\n\n\n<p class=\"has-large-font-size\"><strong><mark style=\"background-color:rgba(0, 0, 0, 0)\" class=\"has-inline-color has-luminous-vivid-orange-color\">29. The IUPAC name of propylene is:<br><\/mark><\/strong>a) But-1-ene<br>b) Ethene<br>c) Prop-1-ene<br>d) But-2-ene<br><strong>Answer:<\/strong> c) Prop-1-ene<br><strong>Explanation:<\/strong> Propylene is prop-1-ene (CH\u2082=CH\u2013CH\u2083).<\/p>\n\n\n\n<p class=\"has-large-font-size\"><strong><mark style=\"background-color:rgba(0, 0, 0, 0)\" class=\"has-inline-color has-luminous-vivid-orange-color\">30. Alkenes mainly undergo:<br><\/mark><\/strong>a) Substitution reactions<br>b) Addition reactions<br>c) Elimination reactions<br>d) Oxidation reactions only<br><strong>Answer:<\/strong> b) Addition reactions<br><strong>Explanation:<\/strong> Double bonds make alkenes reactive towards electrophilic addition.<\/p>\n\n\n\n<p class=\"has-large-font-size\"><strong><mark style=\"background-color:rgba(0, 0, 0, 0)\" class=\"has-inline-color has-luminous-vivid-orange-color\">31. Which of the following is an addition reaction of ethene?<br><\/mark><\/strong>a) Ethene + H\u2082 \u2192 Ethane<br>b) Ethene + Cl\u2082 \u2192 Dichloroethane<br>c) Ethene + HCl \u2192 Chloroethane<br>d) All of the above<br><strong>Answer:<\/strong> d) All of the above<br><strong>Explanation:<\/strong> Alkenes undergo hydrogenation and halogenation addition reactions.<\/p>\n\n\n\n<p class=\"has-large-font-size\"><strong><mark style=\"background-color:rgba(0, 0, 0, 0)\" class=\"has-inline-color has-luminous-vivid-orange-color\">32. The addition of HCl to alkenes follows:<br><\/mark><\/strong>a) Markovnikov\u2019s rule<br>b) Hund\u2019s rule<br>c) Le Chatelier\u2019s principle<br>d) Pauli\u2019s rule<br><strong>Answer:<\/strong> a) Markovnikov\u2019s rule<br><strong>Explanation:<\/strong> According to Markovnikov\u2019s rule, H attaches to carbon with more hydrogens.<\/p>\n\n\n\n<p class=\"has-large-font-size\"><strong><mark style=\"background-color:rgba(0, 0, 0, 0)\" class=\"has-inline-color has-luminous-vivid-orange-color\">33. Anti-Markovnikov addition occurs in the presence of:<br><\/mark><\/strong>a) Peroxides<br>b) Acids<br>c) Alkali metals<br>d) Bases<br><strong>Answer:<\/strong> a) Peroxides<br><strong>Explanation:<\/strong> With peroxides, HBr adds to alkenes in anti-Markovnikov fashion.<\/p>\n\n\n\n<p class=\"has-large-font-size\"><mark style=\"background-color:rgba(0, 0, 0, 0)\" class=\"has-inline-color has-luminous-vivid-orange-color\"><strong>34. Ethene is used in:<\/strong><br><\/mark>a) Welding<br>b) Ripening of fruits<br>c) Rocket fuel<br>d) Anaesthesia<br><strong>Answer:<\/strong> b) Ripening of fruits<br><strong>Explanation:<\/strong> Ethene is a plant hormone that induces fruit ripening.<\/p>\n\n\n\n<p class=\"has-large-font-size\"><strong><mark style=\"background-color:rgba(0, 0, 0, 0)\" class=\"has-inline-color has-luminous-vivid-orange-color\">35. Which reagent is used to test unsaturation in hydrocarbons?<br><\/mark><\/strong>a) Bromine water<br>b) Acidified KMnO\u2084<br>c) Baeyer&#8217;s reagent<br>d) All of these<br><strong>Answer:<\/strong> d) All of these<br><strong>Explanation:<\/strong> Bromine water and Baeyer\u2019s reagent (KMnO\u2084) decolorize with alkenes\/alkynes.<\/p>\n\n\n\n<p class=\"has-large-font-size\"><mark style=\"background-color:rgba(0, 0, 0, 0)\" class=\"has-inline-color has-luminous-vivid-orange-color\"><strong>36. Alkenes on oxidation with cold dilute KMnO\u2084 give:<\/strong><br><\/mark>a) Alcohol<br>b) Diol (glycol)<br>c) Aldehyde<br>d) Ketone<br><strong>Answer:<\/strong> b) Diol (glycol)<br><strong>Explanation:<\/strong> Mild oxidation forms glycols (cis-diols).<\/p>\n\n\n\n<p class=\"has-large-font-size\"><strong><mark style=\"background-color:rgba(0, 0, 0, 0)\" class=\"has-inline-color has-luminous-vivid-orange-color\">37. Ozonolysis of alkenes gives:<br><\/mark><\/strong>a) Alkanes<br>b) Alcohols<br>c) Aldehydes and ketones<br>d) Acids<br><strong>Answer:<\/strong> c) Aldehydes and ketones<br><strong>Explanation:<\/strong> Ozonolysis cleaves double bonds into carbonyl compounds.<\/p>\n\n\n\n<p class=\"has-large-font-size\"><strong><mark style=\"background-color:rgba(0, 0, 0, 0)\" class=\"has-inline-color has-luminous-vivid-orange-color\">38. Alkynes are also called:<br><\/mark><\/strong>a) Acetylenes<br>b) Olefins<br>c) Paraffins<br>d) Aromatics<br><strong>Answer:<\/strong> a) Acetylenes<br><strong>Explanation:<\/strong> Alkynes (CnH\u2082n\u20132) with triple bonds are called acetylenes.<\/p>\n\n\n\n<p class=\"has-large-font-size\"><strong><mark style=\"background-color:rgba(0, 0, 0, 0)\" class=\"has-inline-color has-luminous-vivid-orange-color\">39. General formula of alkynes is:<br><\/mark><\/strong>a) CnH\u2082n+2<br>b) CnH\u2082n<br>c) CnH\u2082n\u20132<br>d) CnH\u2082n\u20131<br><strong>Answer:<\/strong> c) CnH\u2082n\u20132<br><strong>Explanation:<\/strong> Alkynes contain one triple bond, general formula CnH\u2082n\u20132.<\/p>\n\n\n\n<p class=\"has-large-font-size\"><strong><mark style=\"background-color:rgba(0, 0, 0, 0)\" class=\"has-inline-color has-luminous-vivid-orange-color\">40. The first member of alkynes is:<br><\/mark><\/strong>a) Ethyne<br>b) Methyne<br>c) Propyne<br>d) Butyne<br><strong>Answer:<\/strong> a) Ethyne<br><strong>Explanation:<\/strong> Ethyne (C\u2082H\u2082), commonly called acetylene, is the first alkyne.<\/p>\n\n\n\n<p class=\"has-large-font-size\"><strong><mark style=\"background-color:rgba(0, 0, 0, 0)\" class=\"has-inline-color has-luminous-vivid-orange-color\">41. Propyne has molecular formula:<br><\/mark><\/strong>a) C\u2083H\u2084<br>b) C\u2083H\u2086<br>c) C\u2083H\u2088<br>d) C\u2083H\u2082<br><strong>Answer:<\/strong> a) C\u2083H\u2084<br><strong>Explanation:<\/strong> Propyne (HC\u2261C\u2013CH\u2083) has 3 carbons and 4 hydrogens.<\/p>\n\n\n\n<p class=\"has-large-font-size\"><strong><mark style=\"background-color:rgba(0, 0, 0, 0)\" class=\"has-inline-color has-luminous-vivid-orange-color\">42. Alkynes mainly undergo:<br><\/mark><\/strong>a) Addition reactions<br>b) Substitution reactions<br>c) Oxidation only<br>d) Polymerization only<br><strong>Answer:<\/strong> a) Addition reactions<br><strong>Explanation:<\/strong> Alkynes add halogens, hydrogen, and acids across triple bonds.<\/p>\n\n\n\n<p class=\"has-large-font-size\"><strong><mark style=\"background-color:rgba(0, 0, 0, 0)\" class=\"has-inline-color has-luminous-vivid-orange-color\">43. Hydrogenation of ethyne gives:<br><\/mark><\/strong>a) Ethene (partial) \u2192 Ethane (complete)<br>b) Ethane only<br>c) Methane<br>d) Propane<br><strong>Answer:<\/strong> a) Ethene (partial) \u2192 Ethane (complete)<br><strong>Explanation:<\/strong> Ethyne + H\u2082 \u2192 ethene \u2192 ethane.<\/p>\n\n\n\n<p class=\"has-large-font-size\"><strong><mark style=\"background-color:rgba(0, 0, 0, 0)\" class=\"has-inline-color has-luminous-vivid-orange-color\">44. Ethyne reacts with chlorine to form:<br><\/mark><\/strong>a) Dichloroethane<br>b) Tetrachloroethane<br>c) Both (depending on conditions)<br>d) None<br><strong>Answer:<\/strong> c) Both<br><strong>Explanation:<\/strong> Addition of 1 mole Cl\u2082 \u2192 dichloroethene; 2 moles Cl\u2082 \u2192 tetrachloroethane.<\/p>\n\n\n\n<p class=\"has-large-font-size\"><strong><mark style=\"background-color:rgba(0, 0, 0, 0)\" class=\"has-inline-color has-luminous-vivid-orange-color\">45. Which alkyne is used in oxy-acetylene welding?<br><\/mark><\/strong>a) Methyne<br>b) Ethyne<br>c) Propyne<br>d) Butyne<br><strong>Answer:<\/strong> b) Ethyne<br><strong>Explanation:<\/strong> Ethyne burns in oxygen to give high temperature flame (\u2248 3500\u00b0C).<\/p>\n\n\n\n<p class=\"has-large-font-size\"><strong><mark style=\"background-color:rgba(0, 0, 0, 0)\" class=\"has-inline-color has-luminous-vivid-orange-color\">46. Ethyne with ammoniacal AgNO\u2083 gives:<br><\/mark><\/strong>a) White precipitate<br>b) Yellow precipitate<br>c) Brown precipitate<br>d) No reaction<br><strong>Answer:<\/strong> a) White precipitate<br><strong>Explanation:<\/strong> Terminal alkynes form white precipitate of silver acetylide with AgNO\u2083.<\/p>\n\n\n\n<p class=\"has-large-font-size\"><strong><mark style=\"background-color:rgba(0, 0, 0, 0)\" class=\"has-inline-color has-luminous-vivid-orange-color\">47. Ethyne with ammoniacal Cu\u2082Cl\u2082 gives:<br><\/mark><\/strong>a) Red precipitate<br>b) Yellow precipitate<br>c) White precipitate<br>d) Green precipitate<br><strong>Answer:<\/strong> a) Red precipitate<br><strong>Explanation:<\/strong> Terminal alkynes give red precipitate of copper acetylide.<\/p>\n\n\n\n<p class=\"has-large-font-size\"><strong><mark style=\"background-color:rgba(0, 0, 0, 0)\" class=\"has-inline-color has-luminous-vivid-orange-color\">48. Ozonolysis of alkynes gives:<\/mark><\/strong><br>a) Alkanes<br>b) Alcohols<br>c) Carboxylic acids<br>d) Ketones<br><strong>Answer:<\/strong> c) Carboxylic acids<br><strong>Explanation:<\/strong> Triple bond cleavage produces acids.<\/p>\n\n\n\n<p class=\"has-large-font-size\"><strong><mark style=\"background-color:rgba(0, 0, 0, 0)\" class=\"has-inline-color has-luminous-vivid-orange-color\">49. Ethyne reacts with water in presence of H\u2082SO\u2084 and Hg\u00b2\u207a catalyst to form:<br><\/mark><\/strong>a) Ethanol<br>b) Acetaldehyde<br>c) Acetone<br>d) Acetic acid<br><strong>Answer:<\/strong> b) Acetaldehyde<br><strong>Explanation:<\/strong> Hydration of ethyne \u2192 vinyl alcohol \u2192 tautomerizes to acetaldehyde.<\/p>\n\n\n\n<p class=\"has-large-font-size\"><strong><mark style=\"background-color:rgba(0, 0, 0, 0)\" class=\"has-inline-color has-luminous-vivid-orange-color\">50. Which test distinguishes alkanes from alkenes and alkynes?<br><\/mark><\/strong>a) Bromine water test<br>b) Flame test<br>c) Neutralization test<br>d) Distillation<br><strong>Answer:<\/strong> a) Bromine water test<br><strong>Explanation:<\/strong> Alkenes\/alkynes decolorize bromine water; alkanes do not.<\/p>\n\n\n\n<p class=\"has-large-font-size\"><strong><mark style=\"background-color:rgba(0, 0, 0, 0)\" class=\"has-inline-color has-luminous-vivid-orange-color\">51. Aromatic hydrocarbons contain:<br><\/mark><\/strong>a) Only single bonds<br>b) Alternating single and double bonds in a ring<br>c) Only triple bonds<br>d) Open chain carbon atoms<br><strong>Answer:<\/strong> b) Alternating single and double bonds in a ring<br><strong>Explanation:<\/strong> Aromatics follow Huckel\u2019s rule with delocalized \u03c0-electrons.<\/p>\n\n\n\n<p class=\"has-large-font-size\"><strong><mark style=\"background-color:rgba(0, 0, 0, 0)\" class=\"has-inline-color has-luminous-vivid-orange-color\">52. Benzene has the molecular formula:<br><\/mark><\/strong>a) C\u2086H\u2081\u2082<br>b) C\u2086H\u2086<br>c) C\u2086H\u2081\u2080<br>d) C\u2086H\u2088<br><strong>Answer:<\/strong> b) C\u2086H\u2086<br><strong>Explanation:<\/strong> Benzene has 6 carbons and 6 hydrogens, highly unsaturated but stable.<\/p>\n\n\n\n<p class=\"has-large-font-size\"><strong><mark style=\"background-color:rgba(0, 0, 0, 0)\" class=\"has-inline-color has-luminous-vivid-orange-color\">53. The Kekul\u00e9 structure of benzene has:<br><\/mark><\/strong>a) Alternating double and single bonds<br>b) All single bonds<br>c) All double bonds<br>d) No bonds<br><strong>Answer:<\/strong> a) Alternating double and single bonds<br><strong>Explanation:<\/strong> Kekul\u00e9 proposed resonance structures for benzene.<\/p>\n\n\n\n<p class=\"has-large-font-size\"><mark style=\"background-color:rgba(0, 0, 0, 0)\" class=\"has-inline-color has-luminous-vivid-orange-color\"><strong>54. Benzene is considered aromatic because it follows:<\/strong><br><\/mark>a) Le Chatelier\u2019s principle<br>b) Hund\u2019s rule<br>c) Huckel\u2019s rule (4n + 2 \u03c0 electrons)<br>d) Pauli\u2019s principle<br><strong>Answer:<\/strong> c) Huckel\u2019s rule<br><strong>Explanation:<\/strong> Benzene has 6 \u03c0-electrons (n=1) \u2192 aromatic stability.<\/p>\n\n\n\n<p class=\"has-large-font-size\"><strong><mark style=\"background-color:rgba(0, 0, 0, 0)\" class=\"has-inline-color has-luminous-vivid-orange-color\">55. Which of the following is a property of benzene?<br><\/mark><\/strong>a) Highly reactive like alkenes<br>b) Undergoes substitution reactions<br>c) Always undergoes addition reactions<br>d) Combines explosively with water<br><strong>Answer:<\/strong> b) Undergoes substitution reactions<br><strong>Explanation:<\/strong> Aromatics undergo electrophilic substitution instead of addition (stability retained).<\/p>\n\n\n\n<p class=\"has-large-font-size\"><strong><mark style=\"background-color:rgba(0, 0, 0, 0)\" class=\"has-inline-color has-luminous-vivid-orange-color\">56. The main reaction of benzene is:<br><\/mark><\/strong>a) Addition<br>b) Substitution<br>c) Elimination<br>d) Polymerization<br><strong>Answer:<\/strong> b) Substitution<br><strong>Explanation:<\/strong> Benzene maintains aromaticity \u2192 undergoes electrophilic substitution.<\/p>\n\n\n\n<p class=\"has-large-font-size\"><strong><mark style=\"background-color:rgba(0, 0, 0, 0)\" class=\"has-inline-color has-luminous-vivid-orange-color\">57. Nitration of benzene gives:<br><\/mark><\/strong>a) Aniline<br>b) Nitrobenzene<br>c) Phenol<br>d) Benzaldehyde<br><strong>Answer:<\/strong> b) Nitrobenzene<br><strong>Explanation:<\/strong> Benzene + HNO\u2083\/H\u2082SO\u2084 \u2192 nitrobenzene.<\/p>\n\n\n\n<p class=\"has-large-font-size\"><strong><mark style=\"background-color:rgba(0, 0, 0, 0)\" class=\"has-inline-color has-luminous-vivid-orange-color\">58. Sulphonation of benzene gives:<br><\/mark><\/strong>a) Benzaldehyde<br>b) Benzenesulphonic acid<br>c) Nitrobenzene<br>d) Benzyl alcohol<br><strong>Answer:<\/strong> b) Benzenesulphonic acid<br><strong>Explanation:<\/strong> Benzene + SO\u2083\/H\u2082SO\u2084 \u2192 benzenesulphonic acid.<\/p>\n\n\n\n<p class=\"has-large-font-size\"><strong><mark style=\"background-color:rgba(0, 0, 0, 0)\" class=\"has-inline-color has-luminous-vivid-orange-color\">59. Friedel\u2013Crafts alkylation uses:<br><\/mark><\/strong>a) AlCl\u2083 catalyst<br>b) H\u2082SO\u2084 catalyst<br>c) Pt catalyst<br>d) Cu catalyst<br><strong>Answer:<\/strong> a) AlCl\u2083 catalyst<br><strong>Explanation:<\/strong> Alkyl halide + benzene \u2192 alkylbenzene (catalyst AlCl\u2083).<\/p>\n\n\n\n<p class=\"has-large-font-size\"><strong><mark style=\"background-color:rgba(0, 0, 0, 0)\" class=\"has-inline-color has-luminous-vivid-orange-color\">60. Friedel\u2013Crafts acylation introduces:<br><\/mark><\/strong>a) Nitro group<br>b) Alkyl group<br>c) Acyl group (\u2013COR)<br>d) Sulphonic group<br><strong>Answer:<\/strong> c) Acyl group (\u2013COR)<br><strong>Explanation:<\/strong> Acyl halide + benzene + AlCl\u2083 \u2192 acylbenzene.<\/p>\n\n\n\n<p class=\"has-large-font-size\"><strong><mark style=\"background-color:rgba(0, 0, 0, 0)\" class=\"has-inline-color has-luminous-vivid-orange-color\">61. Toluene is:<br><\/mark><\/strong>a) Methylbenzene<br>b) Ethylbenzene<br>c) Dimethylbenzene<br>d) Benzyl alcohol<br><strong>Answer:<\/strong> a) Methylbenzene<br><strong>Explanation:<\/strong> Toluene has a \u2013CH\u2083 group attached to benzene.<\/p>\n\n\n\n<p class=\"has-large-font-size\"><strong><mark style=\"background-color:rgba(0, 0, 0, 0)\" class=\"has-inline-color has-luminous-vivid-orange-color\">62. On nitration, toluene gives mainly:<br><\/mark><\/strong>a) Ortho- and para-nitrotoluene<br>b) Meta-nitrotoluene<br>c) Benzonitrile<br>d) Dinitrobenzene<br><strong>Answer:<\/strong> a) Ortho- and para-nitrotoluene<br><strong>Explanation:<\/strong> \u2013CH\u2083 group is an ortho\/para directing group.<\/p>\n\n\n\n<p class=\"has-large-font-size\"><strong><mark style=\"background-color:rgba(0, 0, 0, 0)\" class=\"has-inline-color has-luminous-vivid-orange-color\">63. Oxidation of toluene with KMnO\u2084 gives:<br><\/mark><\/strong>a) Benzyl alcohol<br>b) Benzaldehyde<br>c) Benzoic acid<br>d) Phenol<br><strong>Answer:<\/strong> c) Benzoic acid<br><strong>Explanation:<\/strong> Side chain oxidation converts \u2013CH\u2083 into \u2013COOH.<\/p>\n\n\n\n<p class=\"has-large-font-size\"><strong><mark style=\"background-color:rgba(0, 0, 0, 0)\" class=\"has-inline-color has-luminous-vivid-orange-color\">64. Xylene is:<br><\/mark><\/strong>a) Dimethylbenzene<br>b) Nitrobenzene<br>c) Benzoic acid<br>d) Aniline<br><strong>Answer:<\/strong> a) Dimethylbenzene<br><strong>Explanation:<\/strong> Xylenes are isomers of C\u2086H\u2084(CH\u2083)\u2082.<\/p>\n\n\n\n<p class=\"has-large-font-size\"><strong><mark style=\"background-color:rgba(0, 0, 0, 0)\" class=\"has-inline-color has-luminous-vivid-orange-color\">65. The number of xylene isomers is:<br><\/mark><\/strong>a) 2<br>b) 3<br>c) 4<br>d) 5<br><strong>Answer:<\/strong> b) 3<br><strong>Explanation:<\/strong> o-xylene, m-xylene, and p-xylene are possible.<\/p>\n\n\n\n<p class=\"has-large-font-size\"><mark style=\"background-color:rgba(0, 0, 0, 0)\" class=\"has-inline-color has-luminous-vivid-orange-color\"><strong>66. Naphthalene consists of:<\/strong><br><\/mark>a) One benzene ring<br>b) Two fused benzene rings<br>c) Three benzene rings<br>d) A benzene + cyclohexane ring<br><strong>Answer:<\/strong> b) Two fused benzene rings<br><strong>Explanation:<\/strong> Naphthalene has two fused aromatic rings.<\/p>\n\n\n\n<p class=\"has-large-font-size\"><strong><mark style=\"background-color:rgba(0, 0, 0, 0)\" class=\"has-inline-color has-luminous-vivid-orange-color\">67. Anthracene contains:<\/mark><\/strong><br>a) 2 benzene rings<br>b) 3 linearly fused benzene rings<br>c) 4 fused benzene rings<br>d) None<br><strong>Answer:<\/strong> b) 3 linearly fused benzene rings<br><strong>Explanation:<\/strong> Anthracene has three fused benzene rings.<\/p>\n\n\n\n<p class=\"has-large-font-size\"><strong><mark style=\"background-color:rgba(0, 0, 0, 0)\" class=\"has-inline-color has-luminous-vivid-orange-color\">68. Phenanthrene contains:<\/mark><\/strong><br>a) 2 fused rings<br>b) 3 fused rings (angular)<br>c) 4 fused rings<br>d) 5 fused rings<br><strong>Answer:<\/strong> b) 3 fused rings (angular)<br><strong>Explanation:<\/strong> Phenanthrene has 3 fused benzene rings in an angular structure.<\/p>\n\n\n\n<p class=\"has-large-font-size\"><strong><mark style=\"background-color:rgba(0, 0, 0, 0)\" class=\"has-inline-color has-luminous-vivid-orange-color\">69. Benzene is less reactive towards addition reactions because:<\/mark><\/strong><br>a) It has high resonance energy<br>b) It is saturated<br>c) It has weak bonds<br>d) It has high reactivity<br><strong>Answer:<\/strong> a) It has high resonance energy<br><strong>Explanation:<\/strong> Resonance stabilizes benzene, preventing addition.<\/p>\n\n\n\n<p class=\"has-large-font-size\"><mark style=\"background-color:rgba(0, 0, 0, 0)\" class=\"has-inline-color has-luminous-vivid-orange-color\"><strong>70. Benzene undergoes chlorination in presence of FeCl\u2083 to give:<\/strong><\/mark><br>a) Chlorobenzene<br>b) Benzyl chloride<br>c) Dichlorobenzene<br>d) Benzene hexachloride<br><strong>Answer:<\/strong> a) Chlorobenzene<br><strong>Explanation:<\/strong> Substitution gives chlorobenzene.<\/p>\n\n\n\n<p class=\"has-large-font-size\"><strong><mark style=\"background-color:rgba(0, 0, 0, 0)\" class=\"has-inline-color has-luminous-vivid-orange-color\">71. Halogenation of benzene requires:<br><\/mark><\/strong>a) UV light<br>b) Lewis acid catalyst (FeCl\u2083, AlCl\u2083)<br>c) H\u2082SO\u2084<br>d) NaOH<br><strong>Answer:<\/strong> b) Lewis acid catalyst (FeCl\u2083, AlCl\u2083)<br><strong>Explanation:<\/strong> Catalysts polarize halogens, enabling substitution.<\/p>\n\n\n\n<p class=\"has-large-font-size\"><strong><mark style=\"background-color:rgba(0, 0, 0, 0)\" class=\"has-inline-color has-luminous-vivid-orange-color\">72. TNT (trinitrotoluene) is prepared from toluene by:<br><\/mark><\/strong>a) Sulphonation<br>b) Nitration<br>c) Halogenation<br>d) Oxidation<br><strong>Answer:<\/strong> b) Nitration<br><strong>Explanation:<\/strong> Toluene nitrated to 2,4,6-trinitrotoluene (explosive).<\/p>\n\n\n\n<p class=\"has-large-font-size\"><strong><mark style=\"background-color:rgba(0, 0, 0, 0)\" class=\"has-inline-color has-luminous-vivid-orange-color\">73. The product of sulphonation of naphthalene at low temperature is:<br><\/mark><\/strong>a) \u03b1-naphthalenesulphonic acid<br>b) \u03b2-naphthalenesulphonic acid<br>c) Nitro-naphthalene<br>d) Naphthol<br><strong>Answer:<\/strong> a) \u03b1-naphthalenesulphonic acid<br><strong>Explanation:<\/strong> Low temperature favours \u03b1-substitution.<\/p>\n\n\n\n<p class=\"has-large-font-size\"><strong><mark style=\"background-color:rgba(0, 0, 0, 0)\" class=\"has-inline-color has-luminous-vivid-orange-color\">74. The product of sulphonation of naphthalene at high temperature is:<br><\/mark><\/strong>a) \u03b1-naphthalenesulphonic acid<br>b) \u03b2-naphthalenesulphonic acid<br>c) Dinitronaphthalene<br>d) Anthracene<br><strong>Answer:<\/strong> b) \u03b2-naphthalenesulphonic acid<br><strong>Explanation:<\/strong> High temperature favours \u03b2-substitution.<\/p>\n\n\n\n<p class=\"has-large-font-size\"><strong><mark style=\"background-color:rgba(0, 0, 0, 0)\" class=\"has-inline-color has-luminous-vivid-orange-color\">75. The most stable aromatic hydrocarbon among the following is:<br><\/mark><\/strong>a) Benzene<br>b) Toluene<br>c) Anthracene<br>d) Naphthalene<br><strong>Answer:<\/strong> a) Benzene<br><strong>Explanation:<\/strong> Benzene has maximum resonance stability compared to fused aromatics.<\/p>\n\n\n\n<p class=\"has-large-font-size\"><strong><mark style=\"background-color:rgba(0, 0, 0, 0)\" class=\"has-inline-color has-luminous-vivid-orange-color\">76. The main source of hydrocarbons is:<br><\/mark><\/strong>a) Air<br>b) Water<br>c) Petroleum and natural gas<br>d) Soil<br><strong>Answer:<\/strong> c) Petroleum and natural gas<br><strong>Explanation:<\/strong> Hydrocarbons are extracted mainly from crude oil and natural gas reserves.<\/p>\n\n\n\n<p class=\"has-large-font-size\"><mark style=\"background-color:rgba(0, 0, 0, 0)\" class=\"has-inline-color has-luminous-vivid-orange-color\"><strong>77. Petroleum is a mixture of:<\/strong><br><\/mark>a) Alkanes only<br>b) Alkanes, cycloalkanes, and aromatics<br>c) Alcohols and acids<br>d) Esters<br><strong>Answer:<\/strong> b) Alkanes, cycloalkanes, and aromatics<br><strong>Explanation:<\/strong> Crude oil contains various hydrocarbons, refined into fuels and chemicals.<\/p>\n\n\n\n<p class=\"has-large-font-size\"><strong><mark style=\"background-color:rgba(0, 0, 0, 0)\" class=\"has-inline-color has-luminous-vivid-orange-color\">78. The process of separating petroleum into useful fractions is:<br><\/mark><\/strong>a) Cracking<br>b) Distillation<br>c) Refining<br>d) Fractional distillation<br><strong>Answer:<\/strong> d) Fractional distillation<br><strong>Explanation:<\/strong> Petroleum is separated by fractional distillation based on boiling points.<\/p>\n\n\n\n<p class=\"has-large-font-size\"><strong><mark style=\"background-color:rgba(0, 0, 0, 0)\" class=\"has-inline-color has-luminous-vivid-orange-color\">79. LPG is a mixture of:<br><\/mark><\/strong>a) Methane and ethane<br>b) Propane and butane<br>c) Ethylene and acetylene<br>d) Benzene and toluene<br><strong>Answer:<\/strong> b) Propane and butane<br><strong>Explanation:<\/strong> LPG (cooking gas) contains mainly propane and butane.<\/p>\n\n\n\n<p class=\"has-large-font-size\"><strong><mark style=\"background-color:rgba(0, 0, 0, 0)\" class=\"has-inline-color has-luminous-vivid-orange-color\">80. CNG mainly contains:<\/mark><\/strong><br>a) Methane<br>b) Ethane<br>c) Propane<br>d) Butane<br><strong>Answer:<\/strong> a) Methane<br><strong>Explanation:<\/strong> Compressed Natural Gas is methane-rich and a clean fuel.<\/p>\n\n\n\n<p class=\"has-large-font-size\"><strong><mark style=\"background-color:rgba(0, 0, 0, 0)\" class=\"has-inline-color has-luminous-vivid-orange-color\">81. Which hydrocarbon is used for welding purposes?<br><\/mark><\/strong>a) Methane<br>b) Ethane<br>c) Ethyne<br>d) Propane<br><strong>Answer:<\/strong> c) Ethyne<br><strong>Explanation:<\/strong> Ethyne (acetylene) burns in oxygen to give a hot flame (~3500\u00b0C).<\/p>\n\n\n\n<p class=\"has-large-font-size\"><strong><mark style=\"background-color:rgba(0, 0, 0, 0)\" class=\"has-inline-color has-luminous-vivid-orange-color\">82. Petrol is obtained from:<br><\/mark><\/strong>a) Light fraction of petroleum<br>b) Heavy fraction of petroleum<br>c) Coal tar<br>d) Natural gas only<br><strong>Answer:<\/strong> a) Light fraction of petroleum<br><strong>Explanation:<\/strong> Petrol (gasoline) comes from lighter fractions during refining.<\/p>\n\n\n\n<p class=\"has-large-font-size\"><strong><mark style=\"background-color:rgba(0, 0, 0, 0)\" class=\"has-inline-color has-luminous-vivid-orange-color\">83. Kerosene belongs to:<br><\/mark><\/strong>a) Lighter fractions of petroleum<br>b) Middle fractions of petroleum<br>c) Heavy fractions of petroleum<br>d) Residue<br><strong>Answer:<\/strong> b) Middle fractions of petroleum<br><strong>Explanation:<\/strong> Kerosene is in the middle distillate range.<\/p>\n\n\n\n<p class=\"has-large-font-size\"><strong><mark style=\"background-color:rgba(0, 0, 0, 0)\" class=\"has-inline-color has-luminous-vivid-orange-color\">84. Diesel is obtained from:<br><\/mark><\/strong>a) Residue<br>b) Middle fraction<br>c) Light fraction<br>d) Gaseous fraction<br><strong>Answer:<\/strong> b) Middle fraction<br><strong>Explanation:<\/strong> Diesel is heavier than kerosene but lighter than lubricating oils.<\/p>\n\n\n\n<p class=\"has-large-font-size\"><strong><mark style=\"background-color:rgba(0, 0, 0, 0)\" class=\"has-inline-color has-luminous-vivid-orange-color\">85. The heaviest fraction obtained from petroleum distillation is:<br><\/mark><\/strong>a) Petrol<br>b) Diesel<br>c) Bitumen<br>d) Kerosene<br><strong>Answer:<\/strong> c) Bitumen<br><strong>Explanation:<\/strong> Bitumen (asphalt) is the residue after fractional distillation.<\/p>\n\n\n\n<p class=\"has-large-font-size\"><strong><mark style=\"background-color:rgba(0, 0, 0, 0)\" class=\"has-inline-color has-luminous-vivid-orange-color\">86. The process of breaking higher hydrocarbons into lower ones is:<br><\/mark><\/strong>a) Polymerization<br>b) Cracking<br>c) Distillation<br>d) Refining<br><strong>Answer:<\/strong> b) Cracking<br><strong>Explanation:<\/strong> Cracking breaks heavy hydrocarbons into lighter alkanes\/alkenes.<\/p>\n\n\n\n<p class=\"has-large-font-size\"><strong><mark style=\"background-color:rgba(0, 0, 0, 0)\" class=\"has-inline-color has-luminous-vivid-orange-color\">87. Which process improves the octane number of petrol?<br><\/mark><\/strong>a) Cracking<br>b) Reforming<br>c) Hydrogenation<br>d) Distillation<br><strong>Answer:<\/strong> b) Reforming<br><strong>Explanation:<\/strong> Catalytic reforming increases branching \u2192 higher octane rating.<\/p>\n\n\n\n<p class=\"has-large-font-size\"><strong><mark style=\"background-color:rgba(0, 0, 0, 0)\" class=\"has-inline-color has-luminous-vivid-orange-color\">88. Polymerization of ethene gives:<br><\/mark><\/strong>a) Polyethene<br>b) Polypropylene<br>c) Polystyrene<br>d) Teflon<br><strong>Answer:<\/strong> a) Polyethene<br><strong>Explanation:<\/strong> Ethene polymerizes to form polyethylene (plastic bags, bottles).<\/p>\n\n\n\n<p class=\"has-large-font-size\"><strong><mark style=\"background-color:rgba(0, 0, 0, 0)\" class=\"has-inline-color has-luminous-vivid-orange-color\">89. Polymerization of propene gives:<br><\/mark><\/strong>a) Polyethene<br>b) Polypropylene<br>c) Polystyrene<br>d) PVC<br><strong>Answer:<\/strong> b) Polypropylene<br><strong>Explanation:<\/strong> Propene polymerizes to polypropylene (ropes, packaging).<\/p>\n\n\n\n<p class=\"has-large-font-size\"><strong><mark style=\"background-color:rgba(0, 0, 0, 0)\" class=\"has-inline-color has-luminous-vivid-orange-color\">90. Polymerization of vinyl chloride gives:<br><\/mark><\/strong>a) PVC<br>b) Polyethene<br>c) Polypropylene<br>d) Nylon<br><strong>Answer:<\/strong> a) PVC<br><strong>Explanation:<\/strong> Vinyl chloride \u2192 polyvinyl chloride (PVC) used in pipes, insulation.<\/p>\n\n\n\n<p class=\"has-large-font-size\"><strong><mark style=\"background-color:rgba(0, 0, 0, 0)\" class=\"has-inline-color has-luminous-vivid-orange-color\">91. Polymerization of styrene gives:<br><\/mark><\/strong>a) Nylon<br>b) Teflon<br>c) Polystyrene<br>d) Polyester<br><strong>Answer:<\/strong> c) Polystyrene<br><strong>Explanation:<\/strong> Styrene polymerizes into polystyrene (disposable cups, packaging).<\/p>\n\n\n\n<p class=\"has-large-font-size\"><strong><mark style=\"background-color:rgba(0, 0, 0, 0)\" class=\"has-inline-color has-luminous-vivid-orange-color\">92. Teflon is obtained by polymerization of:<br><\/mark><\/strong>a) Ethene<br>b) Propene<br>c) Tetrafluoroethene<br>d) Vinyl chloride<br><strong>Answer:<\/strong> c) Tetrafluoroethene<br><strong>Explanation:<\/strong> Teflon (non-stick coating) is PTFE from tetrafluoroethene.<\/p>\n\n\n\n<p class=\"has-large-font-size\"><strong><mark style=\"background-color:rgba(0, 0, 0, 0)\" class=\"has-inline-color has-luminous-vivid-orange-color\">93. The main hydrocarbon in coal gas is:<br><\/mark><\/strong>a) Methane<br>b) Hydrogen<br>c) Carbon monoxide<br>d) A mixture of all<br><strong>Answer:<\/strong> d) A mixture of all<br><strong>Explanation:<\/strong> Coal gas has CH\u2084, H\u2082, and CO.<\/p>\n\n\n\n<p class=\"has-large-font-size\"><strong><mark style=\"background-color:rgba(0, 0, 0, 0)\" class=\"has-inline-color has-luminous-vivid-orange-color\">94. Water gas is a mixture of:<br><\/mark><\/strong>a) CO and H\u2082<br>b) CO\u2082 and H\u2082<br>c) CH\u2084 and CO\u2082<br>d) CO and CH\u2084<br><strong>Answer:<\/strong> a) CO and H\u2082<br><strong>Explanation:<\/strong> Water gas = CO + H\u2082, used as fuel.<\/p>\n\n\n\n<p class=\"has-large-font-size\"><strong><mark style=\"background-color:rgba(0, 0, 0, 0)\" class=\"has-inline-color has-luminous-vivid-orange-color\">95. Producer gas is a mixture of:<br><\/mark><\/strong>a) CO + H\u2082<br>b) CO + N\u2082<br>c) H\u2082 + CH\u2084<br>d) CO\u2082 + N\u2082<br><strong>Answer:<\/strong> b) CO + N\u2082<br><strong>Explanation:<\/strong> Producer gas is CO + N\u2082 from coal with air.<\/p>\n\n\n\n<p class=\"has-large-font-size\"><strong><mark style=\"background-color:rgba(0, 0, 0, 0)\" class=\"has-inline-color has-luminous-vivid-orange-color\">96. Coal tar contains:<br><\/mark><\/strong>a) Alkanes only<br>b) Aromatic hydrocarbons like benzene, naphthalene, anthracene<br>c) Alcohols only<br>d) Acids only<br><strong>Answer:<\/strong> b) Aromatic hydrocarbons<br><strong>Explanation:<\/strong> Coal tar is a source of aromatic hydrocarbons and dyes.<\/p>\n\n\n\n<p class=\"has-large-font-size\"><strong><mark style=\"background-color:rgba(0, 0, 0, 0)\" class=\"has-inline-color has-luminous-vivid-orange-color\">97. The high calorific value of hydrocarbons is due to:<br><\/mark><\/strong>a) Presence of oxygen<br>b) Presence of hydrogen and carbon bonds<br>c) Presence of nitrogen<br>d) Presence of sulphur<br><strong>Answer:<\/strong> b) Presence of hydrogen and carbon bonds<br><strong>Explanation:<\/strong> Hydrocarbons release large energy on combustion (CO\u2082 + H\u2082O).<\/p>\n\n\n\n<p class=\"has-large-font-size\"><strong><mark style=\"background-color:rgba(0, 0, 0, 0)\" class=\"has-inline-color has-luminous-vivid-orange-color\">98. Which hydrocarbon derivative is used as anaesthetic (\u201claughing gas\u201d)?<br><\/mark><\/strong>a) CO<br>b) N\u2082O<br>c) CHCl\u2083<br>d) C\u2082H\u2082<br><strong>Answer:<\/strong> b) N\u2082O<br><strong>Explanation:<\/strong> Nitrous oxide (not a hydrocarbon itself but derivative) is used in anaesthesia.<\/p>\n\n\n\n<p class=\"has-large-font-size\"><strong><mark style=\"background-color:rgba(0, 0, 0, 0)\" class=\"has-inline-color has-luminous-vivid-orange-color\">99. Which hydrocarbon is known as \u201cdry ice\u201d when solidified?<br><\/mark><\/strong>a) Methane<br>b) Carbon dioxide<br>c) Ethane<br>d) Butane<br><strong>Answer:<\/strong> b) Carbon dioxide<br><strong>Explanation:<\/strong> Though CO\u2082 is not a hydrocarbon, it is an important carbon compound often studied alongside fuels.<\/p>\n\n\n\n<p class=\"has-large-font-size\"><mark style=\"background-color:rgba(0, 0, 0, 0)\" class=\"has-inline-color has-luminous-vivid-orange-color\"><strong>100. The main environmental effect of burning hydrocarbons is:<br><\/strong><\/mark>a) Ozone depletion<br>b) Air pollution and greenhouse effect (CO\u2082, CO emissions)<br>c) Soil fertility increase<br>d) Acid rain only<br><strong>Answer:<\/strong> b) Air pollution and greenhouse effect<br><strong>Explanation:<\/strong> Hydrocarbon combustion \u2192 CO\u2082 (global warming), CO, NOx (pollution).<\/p>\n","protected":false},"excerpt":{"rendered":"<p>1. Hydrocarbons are compounds made up of:a) Carbon and oxygenb) Carbon and hydrogenc) Carbon and nitrogend) Carbon and sulphurAnswer: b) Carbon and hydrogenExplanation: Hydrocarbons are organic compounds consisting only of carbon and hydrogen atoms. 2. The simplest hydrocarbon is:a) Methaneb) Ethanec) Propaned) AcetyleneAnswer: a) MethaneExplanation: Methane (CH\u2084) is the first member of alkanes. 3. Alkanes<\/p>\n","protected":false},"author":1,"featured_media":0,"comment_status":"open","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[9],"tags":[16069,15994,15999,16000,16071,16073,16007,15886,15892,15876,15898,15901,15887,15899,15879,15883,16006,16076,15998,16074,10978,15997,4029,15897,5649,5623,15927,16001,15900,16070,15896,16072,16075,15894],"class_list":{"0":"post-12802","1":"post","2":"type-post","3":"status-publish","4":"format-standard","6":"category-chemistry","7":"tag-addition-reactions","8":"tag-alkanes","9":"tag-alkenes","10":"tag-alkynes","11":"tag-aromatic-hydrocarbons","12":"tag-bonding-in-hydrocarbons","13":"tag-chemical-reactions","14":"tag-chemistry-formulas","15":"tag-chemistry-learning","16":"tag-chemistry-mcqs","17":"tag-chemistry-preparation-material","18":"tag-chemistry-questions-and-answers","19":"tag-chemistry-quiz","20":"tag-chemistry-revision","21":"tag-chemistry-study-material","22":"tag-competitive-exam-chemistry","23":"tag-functional-groups","24":"tag-hydrocarbon-applications","25":"tag-hydrocarbons","26":"tag-hydrocarbons-problems","27":"tag-hydrocarbons-top-100-mcqs-with-answer-and-explanation","28":"tag-isomerism","29":"tag-mcqs-adda","30":"tag-mcqs-for-chemistry-exam","31":"tag-mcqs-for-pc-psi-sda-fda-pdo-vao-banking-kas-ias-ssc-gd-ssc-chsl-ssc-cgl-for-all-compitative-exams","32":"tag-mcqs-for-sda-fda-pdo-vao-banking-kas-ias-ssc-gd-ssc-chsl-ssc-cgl-for-all-compitative-exams","33":"tag-molecular-structure","34":"tag-organic-chemistry","35":"tag-psc-chemistry-mcqs","36":"tag-saturated-hydrocarbons","37":"tag-ssc-chemistry-mcqs","38":"tag-substitution-reactions","39":"tag-unsaturated-hydrocarbons","40":"tag-upsc-chemistry-mcqs"},"_links":{"self":[{"href":"https:\/\/mcqsadda.com\/index.php\/wp-json\/wp\/v2\/posts\/12802","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/mcqsadda.com\/index.php\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/mcqsadda.com\/index.php\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/mcqsadda.com\/index.php\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"https:\/\/mcqsadda.com\/index.php\/wp-json\/wp\/v2\/comments?post=12802"}],"version-history":[{"count":3,"href":"https:\/\/mcqsadda.com\/index.php\/wp-json\/wp\/v2\/posts\/12802\/revisions"}],"predecessor-version":[{"id":12955,"href":"https:\/\/mcqsadda.com\/index.php\/wp-json\/wp\/v2\/posts\/12802\/revisions\/12955"}],"wp:attachment":[{"href":"https:\/\/mcqsadda.com\/index.php\/wp-json\/wp\/v2\/media?parent=12802"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/mcqsadda.com\/index.php\/wp-json\/wp\/v2\/categories?post=12802"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/mcqsadda.com\/index.php\/wp-json\/wp\/v2\/tags?post=12802"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}