{"id":618822,"date":"2023-03-04T04:24:14","date_gmt":"2023-03-04T04:24:14","guid":{"rendered":"https:\/\/www.indcareer.com\/schools\/?p=618822"},"modified":"2024-05-02T07:19:50","modified_gmt":"2024-05-02T07:19:50","slug":"ncert-exemplar-class-11-chemistry-chapter-13-hydrocarbons","status":"publish","type":"post","link":"https:\/\/www.indcareer.com\/schools\/ncert-exemplar-class-11-chemistry-chapter-13-hydrocarbons\/","title":{"rendered":"NCERT Exemplar Class 11 Chemistry Chapter 13: Hydrocarbons"},"content":{"rendered":"\n<p>NCERT Exemplar Class 11 Chemistry Chapter 13: Hydrocarbons. NCERT Exemplar Solutions for Class 11 Chemistry Chapter 13 Hydrocarbons prepare students for their Class 11 exams thoroughly. <\/p>\n\n\n\n<p>Chemistry problems and solutions for the Class 11 pdf are provided here which are similar to the questions being asked in the previous year&#8217;s board. <\/p>\n\n\n\n<h2 class=\"wp-block-heading\" id=\"h-ncert-exemplar-class-11-chemistry-chapter-13-hydrocarbons\"><strong>NCERT Exemplar Class 11 Chemistry Chapter 13: Hydrocarbons<\/strong><\/h2>\n\n\n\n<p>Class 11: Chemistry Chapter 13 solutions. Complete Class 11 Chemistry Chapter 13 Notes.<\/p>\n\n\n\n<h3 class=\"wp-block-heading\" id=\"h-multiple-choice-questions-type-i\"><strong>Multiple Choice Questions (Type-I)<\/strong><\/h3>\n\n\n\n<ol class=\"wp-block-list\">\n<li>Arrange the following in decreasing order of their boiling points.<br>(A) n\u2013butane<br>(B) 2\u2013methylbutane<br>(C) n-pentane<br>(D) 2,2\u2013dimethylpropane\n<ul class=\"wp-block-list\">\n<li>(i) A &gt; B &gt; C &gt; D<\/li>\n\n\n\n<li>(ii) B &gt; C &gt; D &gt; A<\/li>\n\n\n\n<li>(iii) D &gt; C &gt; B &gt; A<\/li>\n\n\n\n<li>(iv) C &gt; B &gt; D &gt; A<\/li>\n<\/ul>\n<\/li>\n\n\n\n<li>Arrange the halogens F<sub>2<\/sub>, Cl<sub>2<\/sub>, Br<sub>2<\/sub>, I<sub>2<\/sub>, in order of their increasing reactivity with alkanes.\n<ul class=\"wp-block-list\">\n<li>(i) I<sub>2<\/sub> &lt; Br<sub>2<\/sub> &lt; Cl2 &lt; F<sub>2<\/sub><\/li>\n\n\n\n<li>(ii) Br<sub>2<\/sub> &lt; Cl<sub>2<\/sub> &lt; F2 &lt; I<sub>2<\/sub><\/li>\n\n\n\n<li>(iii) F<sub>2<\/sub> &lt; Cl<sub>2<\/sub> &lt; Br2 &lt; I<sub>2<\/sub><\/li>\n\n\n\n<li>(iv) Br<sub>2<\/sub> &lt; I<sub>2<\/sub> &lt; Cl2 &lt; F<sub>2<\/sub><\/li>\n<\/ul>\n<\/li>\n\n\n\n<li>The increasing order of reduction of alkyl halides with zinc and dilute HCl is\n<ul class=\"wp-block-list\">\n<li>(i) R\u2013Cl &lt; R\u2013I &lt; R\u2013Br<\/li>\n\n\n\n<li>(ii) R\u2013Cl &lt; R\u2013Br &lt; R\u2013I<\/li>\n\n\n\n<li>(iii) R\u2013I &lt; R\u2013Br &lt; R\u2013Cl<\/li>\n\n\n\n<li>(iv) R\u2013Br &lt; R\u2013I &lt; R\u2013Cl<\/li>\n<\/ul>\n<\/li>\n\n\n\n<li>The correct IUPAC name of the following alkane is<br><img decoding=\"async\" src=\"https:\/\/www.indcareer.com\/schools\/wp-content\/uploads\/2023\/03\/15647722207_a32aeafcda_o.jpg\" alt=\"\">\n<ul class=\"wp-block-list\">\n<li>(i) 3,6 \u2013 Diethyl \u2013 2 \u2013 methyloctane<\/li>\n\n\n\n<li>(ii) 5 \u2013 Isopropyl \u2013 3 \u2013 ethyloctane<\/li>\n\n\n\n<li>(iii) 3 \u2013 Ethyl \u2013 5 \u2013 isopropyloctane<\/li>\n\n\n\n<li>(iv) 3 \u2013 Isopropyl \u2013 6 \u2013 ethyloctane<\/li>\n<\/ul>\n<\/li>\n\n\n\n<li>The addition of HBr to 1-butene gives a mixture of products A, B and C<br><img decoding=\"async\" src=\"https:\/\/www.indcareer.com\/schools\/wp-content\/uploads\/2023\/03\/15834431382_1c0cc32bb3_o.jpg\" alt=\"\"><br>The mixture consists of\n<ul class=\"wp-block-list\">\n<li>(i) A and B as major and C as minor products<\/li>\n\n\n\n<li>(ii) B as major, A and C as minor products<\/li>\n\n\n\n<li>(iii) B as minor, A and C as major products<\/li>\n\n\n\n<li>(iv) A and B as minor and C as major products<\/li>\n<\/ul>\n<\/li>\n\n\n\n<li>Which of the following will not show geometrical isomerism ?<br><img decoding=\"async\" src=\"https:\/\/www.indcareer.com\/schools\/wp-content\/uploads\/2023\/03\/15212901524_d2230e13e0_o.jpg\" alt=\"\"><\/li>\n\n\n\n<li>Arrange the following hydrogen halides in order of their decreasing reactivity with propene.\n<ul class=\"wp-block-list\">\n<li>(i) HCl &gt; HBr &gt; HI<\/li>\n\n\n\n<li>(ii) HBr &gt; HI &gt; HCl<\/li>\n\n\n\n<li>(iii) HI &gt; HBr &gt; HCl<\/li>\n\n\n\n<li>(iv) HCl &gt; HI &gt; HBr<\/li>\n<\/ul>\n<\/li>\n\n\n\n<li>Arrange the following carbanions in order of their decreasing stability.<br><img decoding=\"async\" src=\"https:\/\/www.indcareer.com\/schools\/wp-content\/uploads\/2023\/03\/15647063089_f0a8631683_o.jpg\" alt=\"\">\n<ul class=\"wp-block-list\">\n<li>(i) A &gt; B &gt; C<\/li>\n\n\n\n<li>(ii) B &gt; A &gt; C<\/li>\n\n\n\n<li>(iii) C &gt; B &gt; A<\/li>\n\n\n\n<li>(iv) C &gt; A &gt; B<\/li>\n<\/ul>\n<\/li>\n\n\n\n<li>Arrange the following alkyl halides in decreasing order of the rate of \u03b2\u2013 elimination reaction with alcoholic KOH.<br><img decoding=\"async\" src=\"https:\/\/www.indcareer.com\/schools\/wp-content\/uploads\/2023\/03\/15213439693_4076668ce0_o.jpg\" alt=\"\">\n<ul class=\"wp-block-list\">\n<li>(i) A &gt; B &gt; C<\/li>\n\n\n\n<li>(ii) C &gt; B &gt; A<\/li>\n\n\n\n<li>(iii) B &gt; C &gt; A<\/li>\n\n\n\n<li>(iv) A &gt; C &gt; B<\/li>\n<\/ul>\n<\/li>\n\n\n\n<li>Which of the following reactions of methane is incomplete combustion:<br><img decoding=\"async\" src=\"https:\/\/www.indcareer.com\/schools\/wp-content\/uploads\/2023\/03\/15830992671_cf1c09ff54_o.jpg\" alt=\"\"><\/li>\n<\/ol>\n\n\n\n<h3 class=\"wp-block-heading\" id=\"h-multiple-choice-questions-type-ii\"><strong>Multiple Choice Questions (Type-II)<\/strong><\/h3>\n\n\n\n<p><strong>In the following questions two or more options may be correct.<\/strong><\/p>\n\n\n\n<ol class=\"wp-block-list\">\n<li>Some oxidation reactions of methane are given below. Which of them is\/are controlled oxidation reactions?<br><img decoding=\"async\" src=\"https:\/\/www.indcareer.com\/schools\/wp-content\/uploads\/2023\/03\/15830992601_183575de5a_o.jpg\" alt=\"\"><\/li>\n\n\n\n<li>Which of the following alkenes on ozonolysis give a mixture of ketones only?<br><img decoding=\"async\" src=\"https:\/\/www.indcareer.com\/schools\/wp-content\/uploads\/2023\/03\/15212901254_2eb35370e6_o.jpg\" alt=\"\"><\/li>\n\n\n\n<li>Which are the correct IUPAC names of the following compound?<br><img decoding=\"async\" src=\"https:\/\/www.indcareer.com\/schools\/wp-content\/uploads\/2023\/03\/15213439393_a0cd2ee93f_o.jpg\" alt=\"\">\n<ul class=\"wp-block-list\">\n<li>(i) 5\u2013 Butyl \u2013 4\u2013 isopropyldecane<\/li>\n\n\n\n<li>(ii) 5\u2013 Ethyl \u2013 4\u2013 propyldecane<\/li>\n\n\n\n<li>(iii) 5\u2013 sec-Butyl \u2013 4\u2013 iso-propyldecane<\/li>\n\n\n\n<li>(iv) 4\u2013(1-methylethyl)\u2013 5 \u2013 (1-methylpropyl)-decane<\/li>\n<\/ul>\n<\/li>\n\n\n\n<li>Which are the correct IUPAC names of the following compound?<br><img decoding=\"async\" src=\"https:\/\/www.indcareer.com\/schools\/wp-content\/uploads\/2023\/03\/15647721687_183281016b_o.jpg\" alt=\"\">\n<ul class=\"wp-block-list\">\n<li>(i) 5 \u2013 (2\u2032, 2\u2032\u2013Dimethylpropyl)-decane<\/li>\n\n\n\n<li>(ii) 4 \u2013 Butyl \u2013 2,2\u2013 dimethylnonane<\/li>\n\n\n\n<li>(iii) 2,2\u2013 Dimethyl \u2013 4\u2013 pentyloctane<\/li>\n\n\n\n<li>(iv) 5 \u2013 neo Pentyl decane<\/li>\n<\/ul>\n<\/li>\n\n\n\n<li>For an electrophilic substitution reaction, the presence of a halogen atom in the benzene ring _______.\n<ul class=\"wp-block-list\">\n<li>(i) deactivates the ring by inductive effect<\/li>\n\n\n\n<li>(ii) deactivates the ring by resonance<\/li>\n\n\n\n<li>(iii) increases the charge density at ortho and para position relative to meta position by resonance<\/li>\n\n\n\n<li>(iv) directs the incoming electrophile to meta position by increasing the charge density relative to ortho and para position.<\/li>\n<\/ul>\n<\/li>\n\n\n\n<li>In an electrophilic substitution reaction of nitrobenzene, the presence of nitro group ________.\n<ul class=\"wp-block-list\">\n<li>(i) deactivates the ring by inductive effect.<\/li>\n\n\n\n<li>(ii) activates the ring by inductive effect.<\/li>\n\n\n\n<li>(iii) decreases the charge density at ortho and para position of the ring relative to meta position by resonance.<\/li>\n\n\n\n<li>(iv) increases the charge density at meta position relative to the ortho and para positions of the ring by resonance.<\/li>\n<\/ul>\n<\/li>\n\n\n\n<li>Which of the following are correct?<br><img decoding=\"async\" src=\"https:\/\/www.indcareer.com\/schools\/wp-content\/uploads\/2023\/03\/15647444928_8c79b8b301_o.jpg\" alt=\"\"><\/li>\n\n\n\n<li>Four structures are given in options (i) to (iv). Examine them and select the aromatic structures.<br><img decoding=\"async\" src=\"https:\/\/www.indcareer.com\/schools\/wp-content\/uploads\/2023\/03\/15647721667_d867bfcef6_o.jpg\" alt=\"\"><\/li>\n\n\n\n<li>The molecules having dipole moment are __________.\n<ul class=\"wp-block-list\">\n<li>(i) 2,2-Dimethylpropane<\/li>\n\n\n\n<li>(ii) trans-Pent-2-ene<\/li>\n\n\n\n<li>(iii) cis-Hex-3-ene<\/li>\n\n\n\n<li>(iv) 2, 2, 3, 3 \u2013 Tetramethylbutane.<\/li>\n<\/ul>\n<\/li>\n<\/ol>\n\n\n\n<h3 class=\"wp-block-heading\" id=\"h-short-answer-type-questions\"><strong>Short Answer Type Questions<\/strong><\/h3>\n\n\n\n<ol class=\"wp-block-list\">\n<li>Why do alkenes prefer to undergo electrophilic addition reaction while arenes prefer electrophilic substitution reactions? Explain.<\/li>\n\n\n\n<li>Alkynes on reduction with sodium in liquid ammonia form trans alkenes. Will the butene thus formed on reduction of 2-butyne show the geometrical&nbsp;isomerism?<\/li>\n\n\n\n<li>Rotation around carbon-carbon single bond of ethane is not completely free. Justify the statement.<\/li>\n\n\n\n<li>Draw Newman and Sawhorse projections for the eclipsed and staggered conformations of ethane. Which of these conformations is more stable and why?<\/li>\n\n\n\n<li>The intermediate carbocation formed in the reactions of HI, HBr and HCl with propene is the same and the bond energy of HCl, HBr and HI is 430.5 kJ mol<sup>\u20131<\/sup>, 363.7 kJ mol<sup>\u20131<\/sup> and 296.8 kJ mol<sup>\u20131<\/sup> respectively. What will be the order of reactivity of these halogen acids?<\/li>\n\n\n\n<li>What will be the product obtained as a result of the following reaction and why?<br><img decoding=\"async\" src=\"https:\/\/www.indcareer.com\/schools\/wp-content\/uploads\/2023\/03\/15213439303_35c2562ea4_o.jpg\" alt=\"\"><\/li>\n\n\n\n<li>How will you convert benzene into\n<ul class=\"wp-block-list\">\n<li>(i) p \u2013 nitrobromobenzene<\/li>\n\n\n\n<li>(ii) m \u2013 nitrobromobenzene<\/li>\n<\/ul>\n<\/li>\n\n\n\n<li>Arrange the following set of compounds in the order of their decreasing relative reactivity with an electrophile.Give reason.<br><img decoding=\"async\" src=\"https:\/\/www.indcareer.com\/schools\/wp-content\/uploads\/2023\/03\/15809226356_405c9c41ef_o.jpg\" alt=\"\"><\/li>\n\n\n\n<li>Despite their \u2013 I effect, halogens are o- and p-directing in haloarenes. Explain.<\/li>\n\n\n\n<li>Why does presence of a nitro group make the benzene ring less reactive in comparison to the unsubstituted benzene ring. Explain.<\/li>\n\n\n\n<li>Suggest a route for the preparation of nitrobenzene starting from acetylene?<\/li>\n\n\n\n<li>Predict the major product (s) of the following reactions and explain their formation.<br><img decoding=\"async\" src=\"https:\/\/www.indcareer.com\/schools\/wp-content\/uploads\/2023\/03\/15647721607_c5c47e6eba_o.jpg\" alt=\"\"><\/li>\n\n\n\n<li>Nucleophiles and electrophiles are reaction intermediates having electron rich and electron deficient centres respectively. Hence, they tend to attack electron deficient and electron rich centres respectively. Classify the following species as electrophiles and nucleophiles.<br><img decoding=\"async\" src=\"https:\/\/www.indcareer.com\/schools\/wp-content\/uploads\/2023\/03\/15830992221_2d5962535b_o.jpg\" alt=\"\"><\/li>\n\n\n\n<li>The relative reactivity of 1\u00b0, 2\u00b0, 3\u00b0 hydrogen\u2019s towards chlorination is 1 : 3.8 : 5. Calculate the percentages of all monochlorinated products obtained from 2-methylbutane.<\/li>\n\n\n\n<li>Write the structures and names of products obtained in the reactions of sodium with a mixture of 1-iodo-2-methylpropane and 2-iodopropane.<\/li>\n\n\n\n<li>Write hydrocarbon radicals that can be formed as intermediates during monochlorination of 2-methylpropane? Which of them is more stable? Give<br>reasons.<\/li>\n\n\n\n<li>An alkane C<sub>8<\/sub>H<sub>18<\/sub> is obtained as the only product on subjecting a primary alkyl halide to Wurtz reaction. On monobromination this alkane yields a single isomer of a tertiary bromide. Write the structure of alkane and the tertiary bromide.<\/li>\n\n\n\n<li>The ring systems having following characteristics are aromatic.\n<ul class=\"wp-block-list\">\n<li>(i) Planar ring containing conjugated \u03c0 bonds.<\/li>\n\n\n\n<li>(ii) Complete delocalisation of the \u03c0\u2212electrons in ring system i.e. each atom in the ring has unhybridized p-orbital, and<\/li>\n\n\n\n<li>(iii) Presence of (4n+2) \u03c0\u2212electrons in the ring where n is an integer (n = 0, 1, 2,\u2026\u2026\u2026..) [Huckel rule].<br>Using this information classify the following compounds as aromatic\/nonaromatic.<br><img decoding=\"async\" src=\"https:\/\/www.indcareer.com\/schools\/wp-content\/uploads\/2023\/03\/15832863645_3ec4de998e_o.jpg\" alt=\"\"><\/li>\n<\/ul>\n<\/li>\n\n\n\n<li>Which of the following compounds are aromatic according to Huckel\u2019s rule?<br><img decoding=\"async\" src=\"https:\/\/www.indcareer.com\/schools\/wp-content\/uploads\/2023\/03\/15647444748_f4abc860cb_o.jpg\" alt=\"\"><\/li>\n\n\n\n<li>Suggest a route to prepare ethyl hydrogen sulphate (CH<sub>3<\/sub>\u2013CH<sub>2<\/sub>\u2013OSO<sub>2<\/sub>\u2014OH) starting from ethanol (C<sub>2<\/sub>H<sub>5<\/sub>OH).<\/li>\n<\/ol>\n\n\n\n<h3 class=\"wp-block-heading\" id=\"h-matching-type-questions\"><strong>Matching Type Questions<\/strong><\/h3>\n\n\n\n<ol class=\"wp-block-list\">\n<li>Match the reagent from Column I which on reaction with CH<sub>3<\/sub>\u2014CH=CH<sub>2<\/sub> gives some product given in Column II as per the codes given below :<br><img decoding=\"async\" src=\"https:\/\/www.indcareer.com\/schools\/wp-content\/uploads\/2023\/03\/15834430422_29a931fdfb_o.jpg\" alt=\"\"><\/li>\n\n\n\n<li>Match the hydrocarbons in Column I with the boiling points given in Column II.<br><img decoding=\"async\" src=\"https:\/\/www.indcareer.com\/schools\/wp-content\/uploads\/2023\/03\/15648030360_2e45a5b4ef_o.jpg\" alt=\"\"><\/li>\n\n\n\n<li>Match the following reactants in Column I with the corresponding reaction products in Column II.<br><img decoding=\"async\" src=\"https:\/\/www.indcareer.com\/schools\/wp-content\/uploads\/2023\/03\/15830992101_8048cb0cb0_o.jpg\" alt=\"\"><\/li>\n\n\n\n<li>Match the reactions given in Column I with the reaction types in Column II.<br><img decoding=\"async\" src=\"https:\/\/www.indcareer.com\/schools\/wp-content\/uploads\/2023\/03\/15834430262_6291415f91_o.jpg\" alt=\"\"><\/li>\n<\/ol>\n\n\n\n<h3 class=\"wp-block-heading\" id=\"h-assertion-and-reason-type-questions\"><strong>Assertion and Reason Type Questions<\/strong><\/h3>\n\n\n\n<p><strong>In the following questions a statement of assertion (A) followed by a statement of reason (R) is given. Choose the correct option out of the choices given below each question.<\/strong><\/p>\n\n\n\n<ol class=\"wp-block-list\">\n<li>Assertion (A) : The compound cyclooctane has the following structural formula :<br><img decoding=\"async\" src=\"https:\/\/www.indcareer.com\/schools\/wp-content\/uploads\/2023\/03\/1_15647444308_09f4a36596_o.jpg\" alt=\"\"><br>It is cyclic and has conjugated 8\u03c0-electron system but it is not an aromatic compound.<br>Reason (R) : (4n + 2) \u03c0 electrons rule does not hold good and ring is not planar.\n<ul class=\"wp-block-list\">\n<li>(i) Both A and R are correct and R is the correct explanation of A.<\/li>\n\n\n\n<li>(ii) Both A and R are correct but R is not the correct explanation of A.<\/li>\n\n\n\n<li>(iii) Both A and R are not correct.<\/li>\n\n\n\n<li>(iv) A is not correct but R is correct.<\/li>\n<\/ul>\n<\/li>\n\n\n\n<li>Assertion (A) : Toluene on Friedel Crafts methylation gives o\u2013 and p\u2013xylene.<br>Reason (R) : CH<sub>3<\/sub>-group bonded to benzene ring increases electron density at o\u2013 and p\u2013 position.\n<ul class=\"wp-block-list\">\n<li>(i) Both A and R are correct and R is the correct explanation of A.<\/li>\n\n\n\n<li>(ii) Both A and R are correct but R is not the correct explanation of A.<\/li>\n\n\n\n<li>(iii) Both A and R are not correct.<\/li>\n\n\n\n<li>(iv) A is not correct but R is correct.<\/li>\n<\/ul>\n<\/li>\n\n\n\n<li>Assertion (A) : Nitration of benzene with nitric acid requires the use of concentrated sulphuric acid.<br>Reason (R) : The mixture of concentrated sulphuric acid and concentrated nitric acid produces the electrophile, NO<sub>2<\/sub><sup>+<\/sup> .\n<ul class=\"wp-block-list\">\n<li>(i) Both A and R are correct and R is the correct explanation of A.<\/li>\n\n\n\n<li>(ii) Both A and R are correct but R is not the correct explanation of A.<\/li>\n\n\n\n<li>(iii) Both A and R are not correct.<\/li>\n\n\n\n<li>(iv) A is not correct but R is correct.<\/li>\n<\/ul>\n<\/li>\n\n\n\n<li>Assertion (A) : Among isomeric pentanes, 2, 2-dimethylpentane has highest boiling point.<br>Reason (R) : Branching does not affect the boiling point.\n<ul class=\"wp-block-list\">\n<li>(i) Both A and R are correct and R is the correct explanation of A.<\/li>\n\n\n\n<li>(ii) Both A and R are correct but R is not the correct explanation of A.<\/li>\n\n\n\n<li>(iii) Both A and R are not correct.<\/li>\n\n\n\n<li>(iv) A is not correct but R is correct.<\/li>\n<\/ul>\n<\/li>\n<\/ol>\n\n\n\n<h3 class=\"wp-block-heading\" id=\"h-long-answer-type-questions\"><strong>Long Answer Type Questions<\/strong><\/h3>\n\n\n\n<ol class=\"wp-block-list\">\n<li>An alkyl halide C<sub>5<\/sub>H<sub>11<\/sub>Br (A) reacts with ethanolic KOH to give an alkene \u2018B\u2019, which reacts with Br<sub>2<\/sub> to give a compound \u2018C\u2019, which on dehydrobromination gives an alkyne \u2018D\u2019. On treatment with sodium metal in liquid ammonia one mole of \u2018D\u2019 gives one mole of the sodium salt of \u2018D\u2019 and half a mole of hydrogen gas. Complete hydrogenation of \u2018D\u2019 yields a straight chain alkane. Identify A,B, C and D. Give the reactions involved.<\/li>\n\n\n\n<li>896 mL vapour of a hydrocarbon \u2018A\u2019 having carbon 87.80% and hydrogen 12.19% weighs 3.28g at STP. Hydrogenation of \u2018A\u2019 gives 2-methylpentane.<br>Also \u2018A\u2019 on hydration in the presence of H<sub>2<\/sub>SO<sub>4<\/sub> and HgSO<sub>4<\/sub> gives a ketone \u2018B\u2019 having molecular formula C<sub>6<\/sub>H<sub>12<\/sub>O. The ketone \u2018B\u2019 gives a positive iodoform test. Find the structure of \u2018A\u2019 and give the reactions involved.<\/li>\n\n\n\n<li>An unsaturated hydrocarbon \u2018A\u2019 adds two molecules of H<sub>2<\/sub> and on reductive ozonolysis gives butane-1,4-dial, ethanal and propanone. Give the structure of \u2018A\u2019, write its IUPAC name and explain the reactions involved.<\/li>\n\n\n\n<li>In the presence of peroxide addition of HBr to propene takes place according to anti Markovnikov\u2019s rule but peroxide effect is not seen in the case of HCl and HI. Explain.<\/li>\n<\/ol>\n\n\n\n<h3 class=\"wp-block-heading\" id=\"h-answers-to-multiple-choice-questions\"><strong>Answers to Multiple Choice Questions<\/strong><\/h3>\n\n\n\n<figure class=\"wp-block-image\"><img decoding=\"async\" src=\"https:\/\/www.indcareer.com\/schools\/wp-content\/uploads\/2024\/05\/49048585497_a878bcf7ef_o.png\" alt=\"\"\/><\/figure>\n\n\n\n<figure class=\"wp-block-image\"><img decoding=\"async\" src=\"https:\/\/www.indcareer.com\/schools\/wp-content\/uploads\/2024\/05\/49047871963_798e2de1fc_o.png\" alt=\"\"\/><\/figure>\n\n\n\n<figure class=\"wp-block-image\"><img decoding=\"async\" src=\"https:\/\/www.indcareer.com\/schools\/wp-content\/uploads\/2024\/05\/49048376101_a924c24329_o.png\" alt=\"\"\/><\/figure>\n\n\n\n<figure class=\"wp-block-image\"><img decoding=\"async\" src=\"https:\/\/www.indcareer.com\/schools\/wp-content\/uploads\/2024\/05\/49048378511_8ba88df9d2_o.png\" alt=\"\"\/><\/figure>\n\n\n\n<figure class=\"wp-block-image\"><img decoding=\"async\" src=\"https:\/\/www.indcareer.com\/schools\/wp-content\/uploads\/2024\/05\/49047881038_3d25ab4453_o.png\" alt=\"\"\/><\/figure>\n\n\n\n<figure class=\"wp-block-image\"><img decoding=\"async\" src=\"https:\/\/www.indcareer.com\/schools\/wp-content\/uploads\/2024\/05\/49048602837_22cf175d41_o.png\" alt=\"\"\/><\/figure>\n\n\n\n<figure class=\"wp-block-image\"><img decoding=\"async\" src=\"https:\/\/www.indcareer.com\/schools\/wp-content\/uploads\/2024\/05\/49048391531_90182c27cb_o.png\" alt=\"\"\/><\/figure>\n\n\n\n<figure class=\"wp-block-image\"><img decoding=\"async\" src=\"https:\/\/www.indcareer.com\/schools\/wp-content\/uploads\/2024\/05\/49047894453_94768e96a9_o.png\" alt=\"\"\/><\/figure>\n\n\n\n<figure class=\"wp-block-image\"><img decoding=\"async\" src=\"https:\/\/www.indcareer.com\/schools\/wp-content\/uploads\/2024\/05\/49048400896_121d8d8f31_o.png\" alt=\"\"\/><\/figure>\n\n\n\n<figure class=\"wp-block-image\"><img decoding=\"async\" src=\"https:\/\/www.indcareer.com\/schools\/wp-content\/uploads\/2024\/05\/49048619567_14a24be38f_o.png\" alt=\"\"\/><\/figure>\n\n\n\n<figure class=\"wp-block-image\"><img decoding=\"async\" src=\"https:\/\/www.indcareer.com\/schools\/wp-content\/uploads\/2024\/05\/49048626612_99c0a7d0f4_o.png\" alt=\"\"\/><\/figure>\n\n\n\n<figure class=\"wp-block-image\"><img decoding=\"async\" src=\"https:\/\/www.indcareer.com\/schools\/wp-content\/uploads\/2024\/05\/49048415586_21da51ef68_o.png\" alt=\"\"\/><\/figure>\n\n\n\n<figure class=\"wp-block-image\"><img decoding=\"async\" src=\"https:\/\/www.indcareer.com\/schools\/wp-content\/uploads\/2024\/05\/49048632807_175a81c736_o.png\" alt=\"\"\/><\/figure>\n\n\n\n<div class=\"wp-block-buttons is-layout-flex wp-block-buttons-is-layout-flex\">\n<div class=\"wp-block-button\"><a class=\"wp-block-button__link has-background wp-element-button\" href=\"https:\/\/www.indcareer.com\/schools\/ncert-exemplar-problems-solutions\/\" style=\"background-color:#f06d6d\" target=\"_blank\" rel=\"noreferrer noopener\">NCERT Exemplar Solutions<\/a><\/div>\n\n\n\n<div class=\"wp-block-button\"><a class=\"wp-block-button__link has-background wp-element-button\" href=\"https:\/\/www.indcareer.com\/schools\/ncert-exemplar-class-11-Chemistry-solutions\/\" style=\"background-color:#f06d6d\" target=\"_blank\" rel=\"noreferrer noopener\">NCERT Class 11 Exemplar Solutions<\/a><\/div>\n<\/div>\n","protected":false},"excerpt":{"rendered":"<p>NCERT Exemplar Class 11 Chemistry Chapter 13: Hydrocarbons. NCERT Exemplar Solutions for Class 11 Chemistry Chapter 13 Hydrocarbons prepare students for their Class 11 exams thoroughly. Chemistry problems and solutions for the Class 11 pdf are provided here which are similar to the questions being asked in the previous year&#8217;s board. NCERT Exemplar Class 11 [&hellip;]<\/p>\n","protected":false},"author":302,"featured_media":618867,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"newspack_featured_image_position":"","newspack_post_subtitle":"","newspack_article_summary_title":"Overview:","newspack_article_summary":"","newspack_hide_updated_date":false,"newspack_show_updated_date":false,"footnotes":""},"categories":[1411,919],"tags":[],"boards":[],"class_list":["post-618822","post","type-post","status-publish","format-standard","has-post-thumbnail","hentry","category-book-solutions","category-class-11","entry"],"yoast_head":"<!-- This site is optimized with the Yoast SEO Premium plugin v27.0 (Yoast SEO v27.1.1) - https:\/\/yoast.com\/product\/yoast-seo-premium-wordpress\/ -->\n<title>NCERT Exemplar for Class 11, Chemistry Chapter 13 - IndCareer Schools<\/title>\n<meta name=\"description\" content=\"NCERT Exemplar Class 11 Chemistry Chapter 13: Hydrocarbons | Browse all Class 11 Chemistry Chapters NCERT Exemplar books - IndCareer Schools\" \/>\n<meta name=\"robots\" content=\"index, follow, max-snippet:-1, max-image-preview:large, max-video-preview:-1\" \/>\n<link rel=\"canonical\" href=\"https:\/\/www.indcareer.com\/schools\/ncert-exemplar-class-11-chemistry-chapter-13-hydrocarbons\/\" \/>\n<meta property=\"og:locale\" content=\"en_US\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"NCERT Exemplar Class 11 Chemistry Chapter 13: Hydrocarbons\" \/>\n<meta property=\"og:description\" content=\"NCERT Exemplar Class 11 Chemistry Chapter 13: Hydrocarbons. NCERT Exemplar Solutions for Class 11 Chemistry Chapter 13 Hydrocarbons prepare students for\" \/>\n<meta property=\"og:url\" content=\"https:\/\/www.indcareer.com\/schools\/ncert-exemplar-class-11-chemistry-chapter-13-hydrocarbons\/\" \/>\n<meta property=\"og:site_name\" content=\"IndCareer Schools\" \/>\n<meta property=\"article:publisher\" content=\"https:\/\/www.facebook.com\/indcareer\" \/>\n<meta property=\"article:published_time\" content=\"2023-03-04T04:24:14+00:00\" \/>\n<meta property=\"article:modified_time\" content=\"2024-05-02T07:19:50+00:00\" \/>\n<meta property=\"og:image\" content=\"https:\/\/www.indcareer.com\/schools\/wp-content\/uploads\/2023\/03\/indcareer-schools-2-24-scaled.jpg\" \/>\n\t<meta property=\"og:image:width\" content=\"1600\" \/>\n\t<meta property=\"og:image:height\" content=\"901\" \/>\n\t<meta property=\"og:image:type\" content=\"image\/jpeg\" \/>\n<meta name=\"author\" content=\"Pooja\" \/>\n<meta name=\"twitter:card\" content=\"summary_large_image\" \/>\n<meta name=\"twitter:creator\" content=\"@indcareer\" \/>\n<meta name=\"twitter:site\" content=\"@indcareer\" \/>\n<meta name=\"twitter:label1\" content=\"Written by\" \/>\n\t<meta name=\"twitter:data1\" content=\"Pooja\" \/>\n\t<meta name=\"twitter:label2\" content=\"Est. reading time\" \/>\n\t<meta name=\"twitter:data2\" content=\"16 minutes\" \/>\n<script type=\"application\/ld+json\" class=\"yoast-schema-graph\">{\"@context\":\"https:\/\/schema.org\",\"@graph\":[{\"@type\":\"Article\",\"@id\":\"https:\/\/www.indcareer.com\/schools\/ncert-exemplar-class-11-chemistry-chapter-13-hydrocarbons\/#article\",\"isPartOf\":{\"@id\":\"https:\/\/www.indcareer.com\/schools\/ncert-exemplar-class-11-chemistry-chapter-13-hydrocarbons\/\"},\"author\":{\"name\":\"Pooja\",\"@id\":\"https:\/\/www.indcareer.com\/schools\/#\/schema\/person\/d6945cf059726f162259ba738092301e\"},\"headline\":\"NCERT Exemplar Class 11 Chemistry Chapter 13: Hydrocarbons\",\"datePublished\":\"2023-03-04T04:24:14+00:00\",\"dateModified\":\"2024-05-02T07:19:50+00:00\",\"mainEntityOfPage\":{\"@id\":\"https:\/\/www.indcareer.com\/schools\/ncert-exemplar-class-11-chemistry-chapter-13-hydrocarbons\/\"},\"wordCount\":1777,\"publisher\":{\"@id\":\"https:\/\/www.indcareer.com\/schools\/#organization\"},\"image\":{\"@id\":\"https:\/\/www.indcareer.com\/schools\/ncert-exemplar-class-11-chemistry-chapter-13-hydrocarbons\/#primaryimage\"},\"thumbnailUrl\":\"https:\/\/www.indcareer.com\/schools\/wp-content\/uploads\/2023\/03\/indcareer-schools-2-24-scaled.jpg\",\"articleSection\":[\"Book Solutions\",\"class 11\"],\"inLanguage\":\"en-US\"},{\"@type\":\"WebPage\",\"@id\":\"https:\/\/www.indcareer.com\/schools\/ncert-exemplar-class-11-chemistry-chapter-13-hydrocarbons\/\",\"url\":\"https:\/\/www.indcareer.com\/schools\/ncert-exemplar-class-11-chemistry-chapter-13-hydrocarbons\/\",\"name\":\"NCERT Exemplar for Class 11, Chemistry Chapter 13 - 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