Chapter 26

A Complete Resource Book in Chemistry for JEE Main · 131 exercises

Problem 62

Wurtz reaction involves the reduction of alkyl halide with (a) HI (b) \(\mathrm{Zn} / \mathrm{HCl}\) (c) Zn in an inert solvent (d) Na in ether

3 step solution

Problem 63

Which of the following compound reacts with chlorobenzene to produce DDT? (a) trichloroacetaldehyde (b) m-chloroacetaldehyde (c) acetaldehyde (d) nitrobenzene

4 step solution

Problem 64

Chloroform is slowly oxidized by air in the presence of light and air to form (a) phosgene (b) formyl chloride (c) formaldehyde (d) trichloroethanol

4 step solution

Problem 67

The reaction of the formation of bromobenzyl chloride with \(\mathrm{NaCN}\) in ethanol leads to (a) 4-bromo-2-cyanobenzyl chloride (b) 4 -cyanobenzyl cyanide (c) 4-cyanobenzyl chloride (d) 4-bromobenzyl cyanide

4 step solution

Problem 72

\(\mathrm{CH}_{3}-\mathrm{CH}_{2}-\mathrm{CH}_{2}-\mathrm{Cl} \stackrel{\text { alc. } \mathrm{KOH}}{\longrightarrow}(\mathrm{X}) \stackrel{\mathrm{HBr}}{\longrightarrow}(\mathrm{Y}) \stackrel{\mathrm{Na} \text { /ether }}{\longrightarrow}(\mathrm{Z})\) In the above sequence of reaction, the product (Z) is (a) propane (b) hexane (c) 2,3 -dimethylbutane (d) allyl bromide

3 step solution

Problem 73

\(\mathrm{R}-\mathrm{OH}+\mathrm{HX} \longrightarrow \mathrm{R}-\mathrm{X}+\mathrm{H}_{2} \mathrm{O}\) In the above reaction, the reactivity of different alcohols is (a) tertiary > secondary > primary (b) tertiary \(>\) secondary \(<\) primary (c) tertiary \(<\) secondary \(>\) primary (d) secondary < primary \(<\) tertiary

5 step solution

Problem 74

Under which of the following conditions would toluene \(\mathrm{C}_{6} \mathrm{H}_{5}-\mathrm{CH}_{3}\), be converted into bromomethyl ben8 zene, \(\mathrm{C}_{6} \mathrm{H}_{5}-\mathrm{CH}_{2} \mathrm{Br} ?\) (a) reaction with \(\mathrm{Br}_{2}\) in dark (b) reaction with \(\mathrm{Br}_{2} / \mathrm{FeBr}_{3}\) (c) reaction with \(\mathrm{Br}_{2}\) in sunlight (d) reaction with \(\mathrm{HBr}\)

6 step solution

Problem 75

The number of isomeric alkyl halides possible for \(\mathrm{C}_{5} \mathrm{H}_{11} \mathrm{Cl}\) is (a) 5 (b) 6 (c) 4 (d) 8

6 step solution

Problem 76

The following transformation proceed through O=[N+]([O-])c1ccc(Cl)c([N+](=O)[O-])c1 O=[N+]([O-])c1ccc([N+](=O)[O-])c([N+](=O)[O-])c1 (a) benzyne intermediate (b) oxirane (c) electrophillic addition (d) activated nucleophillic substitution

4 step solution

Problem 77

Chlorination of toluene in the presence of light and heat followed by treatment with aqueous \(\mathrm{NaOH}\) gives (a) p-cresol (b) o-cresol (c) benzoic acid (d) 2,4 -dihydroxytoluene

5 step solution

Problem 79

The reaction of benzyl chloride with sodium cyanide followed by reduction with hydrogen in the presence of nickel gives (a) n-isobutylaniline (b) \(\beta\)-phenylethylamine (c) aniline (d) benzylamine

4 step solution

Problem 80

Identify \(Z\) in the following series: \(\mathrm{C}_{2} \mathrm{H}_{5} \mathrm{I} \stackrel{\mathrm{Alc} . \mathrm{KOH}}{\longrightarrow} \mathrm{X} \stackrel{\mathrm{Br}_{2}}{\longrightarrow \mathrm{Y}} \stackrel{\mathrm{KCN}}{\longrightarrow} \mathrm{Z}\) (a) \(\mathrm{CH}_{3} \mathrm{CH}_{2} \mathrm{CN}\) (b) \(\mathrm{NCCH}_{2}-\mathrm{CH}_{2} \mathrm{CN}\) (c) \(\mathrm{BrCH}_{2}-\mathrm{CH}_{2} \mathrm{CN}\) (d) \(\mathrm{BrCH}=\mathrm{CHCN}\)

5 step solution

Problem 81

Which of the following represents the correct order of densities? (a) \(\mathrm{CCl}_{4}>\mathrm{CHCl}_{3}>\mathrm{CH}_{2} \mathrm{Cl}_{2}>\mathrm{CH}_{3} \mathrm{Cl}>\mathrm{H}_{2} \mathrm{O}\) (b) \(\mathrm{CCl}_{4}>\mathrm{CHCl}_{3}>\mathrm{CH}_{2} \mathrm{Cl}_{2}>\mathrm{H}_{2} \mathrm{O}>\mathrm{CH}_{3} \mathrm{Cl}\) (c) \(\mathrm{H}_{2} \mathrm{O}>\mathrm{CH}_{3} \mathrm{Cl}>\mathrm{CH}_{2} \mathrm{Cl}_{2}>\mathrm{CHCl}_{3}>\mathrm{CCl}_{4}\) (d) \(\mathrm{CCl}_{4}>\mathrm{CHCl}_{3}>\mathrm{H}_{2} \mathrm{O}>\mathrm{CH}_{2} \mathrm{Cl}_{2}>\mathrm{CH}_{3} \mathrm{Cl}\)

4 step solution

Problem 82

Which of the following is an example of \(\mathrm{S}_{\mathrm{N}^{2}}\) reaction? (a) \(\mathrm{CH}_{3} \mathrm{Br}+\mathrm{OH}^{-} \longrightarrow \mathrm{CH}_{3} \mathrm{OH}+\mathrm{Br}\) (b) CC(Br)CC(CO)CBr (c) \(\mathrm{CH}_{3}-\mathrm{CH}_{2}-\mathrm{OH} \underset{2}{\mathrm{Heat}} \mathrm{H}_{2} \mathrm{O}+\mathrm{H}_{2} \mathrm{C}=\mathrm{CH}_{2}\) (d)

3 step solution

Problem 83

The compound \(\mathrm{C}\) in the following is sequence: \(\mathrm{C}_{7} \mathrm{H}_{8} \stackrel{3 \mathrm{Cl}_{2} / \Delta}{\longrightarrow} \mathrm{A} \stackrel{\mathrm{Br}_{2} / \mathrm{Fe}}{\longrightarrow} \mathrm{B} \stackrel{\mathrm{Zn} / \mathrm{HCl}}{\rightarrow} \mathrm{C}\) (a) p-bromotoluene (b) o-bromotoluene (c) m-bromotoluene (d) 3 -bromo-2, 4,6 -trichlorotoluene

4 step solution

Problem 85

The pesticide DDT slowly changes to (a) p, p-dichlorodiphenyldichloroethene (b) p, p'-dichlorodiphenyldichloroethane (c) p, p'-dichlorodiphenylethene (d) \(\mathrm{CCl}_{3}-\mathrm{CHO}\) and chlorobenzene

4 step solution

Problem 86

Iodoform on heating with KOH gives (a) \(\mathrm{CH}_{3} \mathrm{COOK}\) (b) HCOOK (c) \(\mathrm{HCHO}\) (d) \(\mathrm{CH}_{3} \mathrm{CHO}\)

4 step solution

Problem 87

When chlorine is passed through propene at \(400^{\circ} \mathrm{C}\), which of the following is formed? (a) allyl chloride (b) PVC (c) vinyl chloride (d) 1,2 -dichloroethane

4 step solution

Problem 88

\(\left(\mathrm{CH}_{3}\right)_{3} \mathrm{C}-\mathrm{Cl} \stackrel{\text { Acl. } \mathrm{KOH}}{\Delta} \rightarrow \mathrm{A} \frac{\mathrm{SO}_{2} \mathrm{Cl}_{2}}{475 \mathrm{~K}}-\mathrm{B}\) The compound \(\mathrm{B}\) in the above sequence is (a) 1,2 -dichloro-2-methyl propene (b) 1 -chloro-2-methyl propene (c) 1,2 -dichloro-2-methyl propene (d) 3 -chloro-2-methyl propene

4 step solution

Problem 89

An alkyl chloride produces a single alkene on reaction with sodium ethoxide and ethanol. The alkene further undergoes hydrogenation to yield 2 -methylbutane. Identify the alkyl chloride from amongst the following. (a) \(\mathrm{ClCH}_{2} \mathrm{CH}\left(\mathrm{CH}_{3}\right) \mathrm{CH}_{2} \mathrm{CH}_{3}\) (b) \(\mathrm{ClCH}_{2} \mathrm{C}\left(\mathrm{CH}_{3}\right)_{2} \mathrm{CH}_{3}\) (c) \(\mathrm{ClCH}_{2} \mathrm{CH}_{2} \mathrm{CH}_{2} \mathrm{CH}_{3}\) (d) \(\mathrm{CH}_{3} \mathrm{C}(\mathrm{Cl})\left(\mathrm{CH}_{3}\right) \mathrm{CH}_{2} \mathrm{CH}_{3}\)

4 step solution

Problem 91

In the following groups: 1\. \(-\mathrm{OAc}\) 2\. - OMe 3\. \(-\mathrm{OSO}_{2} \mathrm{Me}\) 4\. \(-\mathrm{OSO}_{2} \mathrm{CF}_{3}\) the order of leaving group ability is (a) \(1>2>3>4\) (b) \(4>3>1>2\) (c) \(4>2>1>3\) (d) \(2>3>4>1\)

4 step solution

Problem 92

At higher temperature, iodoform reaction is given by (a) \(\mathrm{CH}_{3} \mathrm{CO}_{2} \mathrm{CH}_{3}\) (b) \(\mathrm{CH}_{3} \mathrm{CO}_{2} \mathrm{C}_{6} \mathrm{H}_{5}\) (c) \(\mathrm{CH}_{3} \mathrm{CO}_{2} \mathrm{C}_{2} \mathrm{H}_{5}\) (d) \(\mathrm{C}_{6} \mathrm{H}_{3} \mathrm{CO}_{2} \mathrm{CH}_{3}\)

6 step solution

Problem 93

Allyl chloride on dehydrochlorination gives (a) propylene (b) acetone (c) propadiene (d) allyl alcohol

4 step solution

Problem 94

Identify \(Z\) in the following series: \(\mathrm{CH}_{2}=\mathrm{CH}_{2} \stackrel{\mathrm{HBr}}{\longrightarrow} \mathrm{X} \stackrel{\text { Hydrolysis }}{\longrightarrow} \mathrm{Y} \stackrel{\mathrm{I}_{2}, \text { Excess }}{\longrightarrow} \mathrm{Z}\) (a) \(\mathrm{CHI}_{3}\) (b) \(\mathrm{CH}_{3} \mathrm{CHO}\) (c) \(\mathrm{C}_{2} \mathrm{H}_{5} \mathrm{I}\) (d) \(\mathrm{C}_{2} \mathrm{H}_{3} \mathrm{OH}\)

3 step solution

Problem 96

The order of reactivities of the following alklyl halides for a \(\mathrm{S}_{\mathrm{N}}^{2}\) reaction is (a) \(\mathrm{RF}>\mathrm{RCl}>\mathrm{RBr}>\mathrm{RI}\) (b) \(\mathrm{RF}>\mathrm{RBr}>\mathrm{RCl}>\mathrm{RI}\) (c) \(\mathrm{RCl}>\mathrm{RBr}>\mathrm{RF}>\mathrm{RI}\) (d) \(\mathrm{RI}>\mathrm{RBr}>\mathrm{RCl}>\mathrm{RF}\)

3 step solution

Problem 98

During debromination of meso-dibromobutane, the major compound formed is (a) \(\mathrm{n}\)-butane (b) 1 -butane (c) cis-2-butene (d) trans-2-butene

4 step solution

Problem 100

The products formed when alcoholic silver nitrile reacts with ethyl bromide are 1\. ethyne 2\. ethene 3\. nitroethane 4\. ethyl alcohol 5\. ethyl nitrile (a) 3,5 (b) 3,4 (c) \(2,3,5\) (d) 1,5

5 step solution

Problem 101

1-chlorobutane on reaction with alcoholic potash gives (a) 1 -butene (b) 1 -butanol (c) 2 -butene (d) 2-butanol

4 step solution

Problem 102

n-propyl bromide on treatment with ethanolic potassium hydroxide produces (a) propane (b) propene (c) propyne (d) propanol

4 step solution

Problem 103

Which one of the following compounds undergoes substitution at a slower rate than benzene and yet yields predominantly ortho and para products? (a) phenol (b) chlorobenzene (c) nitrobenzene (d) benzene sulphonic acid

5 step solution

Problem 104

Reaction of ethyl benzene with bromine in presence of \(\mathrm{FeBr}_{3}\) gives (a) 2-bromoethyl benzene (b) 2 -bromoethyl benzene (c) 3-bromoethyl benzene (d) 4 -bromoethyl benzene

4 step solution

Problem 105

An organic compound \(\mathrm{X}\left(\mathrm{C}_{4} \mathrm{H}_{9} \mathrm{Cl}\right)\) on reaction with \(\mathrm{Na} /\) diethylether gives a hydrocarbon which on monochlorination gives only one chloro derivative then, \(\mathrm{X}\) is (a) t-butyl chloride (b) s-butyl chloride (c) iso-butyl chloride (d) \(\mathrm{n}\)-butyl chloride

4 step solution

Problem 106

Propyl benzene reacts with bromine in presence of light or heat to give (a) CC(Br)Cc1ccccc1 (b) CCC(Br)c1ccccc1 (c) CCCc1ccccc1Br (d) BrCCCc1ccccc1

4 step solution

Problem 107

Identify the final product (C) in the following sequence of reactions. \(\mathrm{CH}_{3} \mathrm{CH}_{2} \mathrm{I} \stackrel{\text { Alc. } \mathrm{KOH}, \Delta}{\longrightarrow}(\mathrm{A}) \stackrel{\mathrm{Br}_{2}}{\longrightarrow}(\mathrm{B}) \stackrel{\mathrm{KCN}}{\longrightarrow}(\mathrm{C})\) (a) \(\mathrm{NCCH}_{2} \mathrm{CH}_{2} \mathrm{CN}\) (b) \(\mathrm{CH}_{3} \mathrm{CH}_{2} \mathrm{Br}\) (c) \(\mathrm{CH}_{3} \mathrm{CH}_{2} \mathrm{CN}\) (d) \(\mathrm{BrCH}_{2} \mathrm{CH}_{2} \mathrm{CN}\)

3 step solution

Problem 108

Consider the following sequence of reactions \(\left(\mathrm{CH}_{3}\right)_{2} \mathrm{CHBr} \stackrel{\text { Ethanolic } \mathrm{KOH}}{\longrightarrow}(\mathrm{X}) \stackrel{\mathrm{Br}_{2}}{\longrightarrow}(\mathrm{Y})\) \(\frac{\mathrm{NaNH}_{2}}{\mathrm{liq} \cdot \mathrm{NH}_{3}}(\mathrm{Z})\) The end product \((Z)\) is (a) propane (b) propyne (c) propene (d) propan-2-al

3 step solution

Problem 109

Which one is the correct statement? (a) 2-butene is Saytzeff's product (b) 1-butene is the Hofmann product (c) both (a) and (b) are correct (d) none is correct

4 step solution

Problem 110

Replacement of \(\mathrm{Cl}\) of chlorobenzene to give phenol requires drastic conditions, but chlorine of 2,4 dinitrochlorobenzene is readily replaced because (a) \(-\mathrm{NO}_{2}\) makes the ring electron rich at ortho and para positions (b) \(-\mathrm{NO}_{2}\) withdraws electrons at meta position (c) \(-\mathrm{NO}_{2}\) donates electrons at meta position (d) \(-\mathrm{NO}_{2}\) withdraws electrons at ortho and para positions

4 step solution

Problem 114

The refluxing of the silver salt of the carboxylic acid in \(\mathrm{CCl}_{4}\) to form haloalkane or haloarene is called (a) Friedel-Crafts reaction (b) Wittig reaction (c) Hoffmann's bromamide reaction (d) Hunsdiecker reaction

4 step solution

Problem 115

A compound \(\mathrm{P}\left(\mathrm{C}_{3} \mathrm{H}_{6} \mathrm{Cl}_{2}\right)\) on reaction with an alkali either gives a compound \(\mathrm{Q}\left(\mathrm{C}_{3} \mathrm{H}_{6} \mathrm{O}\right)\) or \(\mathrm{R}\left(\mathrm{C}_{3} \mathrm{H}_{4}\right)\). On oxidation, Q gives a compound \(\mathrm{C}_{3} \mathrm{H}_{6} \mathrm{O}_{2} . \mathrm{R}\), on reacting with dilute \(\mathrm{H}_{2} \mathrm{SO}_{4}\) containing \(\mathrm{Hg}^{2+}\) ion, gives a compound \(\mathrm{S}\left(\mathrm{C}_{3} \mathrm{H}_{6} \mathrm{O}\right)\), which reacts with bromine and alkali to give sodium salt of \(\mathrm{C}_{2} \mathrm{H}_{4} \mathrm{O}_{2}\). Then \(\mathrm{P}\) is (a) \(\mathrm{CH}_{2} \mathrm{ClCH}_{2} \mathrm{CH}_{2} \mathrm{Cl}\) (b) \(\mathrm{CH}_{3} \mathrm{CCl}_{2} \mathrm{CH}_{3}\) (c) \(\mathrm{CH}_{3} \mathrm{CHClCH}_{2} \mathrm{Cl}\) (d) \(\mathrm{CH}_{3} \mathrm{CH}_{2} \mathrm{CHCl}_{2}\)

3 step solution

Problem 120

Which of the following statements is/are correct? 1\. \(\mathrm{CH}_{3} \mathrm{CHCl} . \mathrm{CH}_{3}\) is a secondary alkyl halide. 2\. Acetylene is formed when \(\mathrm{CH}_{2}=\mathrm{CH}-\mathrm{Cl}\) is heated with water. 3\. Iodoform gives a precipitate with \(\mathrm{AgNO}_{3}\) solution on heating, whereas chloroform does not. 4\. Freon \(\left(\mathrm{CCl}_{2} \mathrm{~F}_{2}\right)\) is prepared by the action of \(\mathrm{CCl}_{4}\) and \(\mathrm{SbF}_{3}\) in the presence of \(\mathrm{SbCl}_{5}\) as a catalyst. (a) 1,2 and 3 (b) 2,3 and 4 (c) 1,3 and 4 (d) 3 and 4

4 step solution

Problem 121

Which of the following pair is correctly matched? List I List II (Reaction) \(\quad\) (Product) I. \(\mathrm{RX}+\mathrm{AgCN} \quad \mathrm{RNC}\) II. RX + KCN \(\quad\) RCN III. \(\mathrm{RX}+\mathrm{KNO}_{2} \mathrm{R}-\mathrm{N} \leqslant_{\mathrm{O}}^{\nearrow \mathrm{O}}\) IV. \(\mathrm{RX}+\mathrm{AgNO}_{2} \quad \mathrm{R}-\mathrm{O}-\mathrm{N}=\mathrm{O}\) Select the correct answer using the codes given bels (a) I and II (b) III and IV (c) I only (d) I, II, III and IV

6 step solution

Problem 122

The decreasing order of reactivity of I. m-nitrobromobenzene II. \(2,4,6\)-trinitrobromobenzene III. p-nitrobromobenzene IV. and 2,4 -dinitrobromobenzene towards \(\mathrm{OH}^{-}\)ions is (a) \(\mathrm{I}>\mathrm{II}>\mathrm{III}>\mathrm{IV}\) (b) \(\mathrm{II}>\mathrm{IV}>\mathrm{I}>\mathrm{III}\) (c) \(\mathrm{II}>\mathrm{IV}>\mathrm{III}>\mathrm{I}\) (d) IV \(>\mathrm{II}>\mathrm{III}>\mathrm{I}\)

4 step solution

Problem 123

Arrange the following halides in the decreasing order of \(\mathrm{S}_{\mathrm{N}}^{1}\) reactivity. I. \(\mathrm{CH}_{3} \mathrm{CH}_{2} \mathrm{CH}_{2} \mathrm{Cl}\) II. \(\mathrm{CH}_{2}=\mathrm{CHCH}(\mathrm{Cl}) \mathrm{CH}_{3}\) III. \(\mathrm{CH}_{3} \mathrm{CH}_{2} \mathrm{CH}(\mathrm{Cl}) \mathrm{CH}_{3}\) (a) \(\mathrm{I}>\mathrm{II}>\mathrm{III}\) (b) \(\mathrm{II}>\mathrm{III}>\mathrm{I}\) (c) \(\mathrm{II}>\mathrm{I}>\mathrm{III}\) (d) \(\mathrm{III}>\mathrm{II}>\mathrm{I}\)

5 step solution

Problem 124

Match List I (compound) with List II (use) and select the correct answer using the codes given below the lists: List I List II (Compound) (Use) I. acetylsalicylic A. insecticide II. DDT B. drug III. naphthalene C. moth repellent IV. carbon tetrachloride D. fire extinguisher E. refrigerant (a) I-E, II-A, III-C, IV-D (b) \(\mathrm{I}-\mathrm{B}, \mathrm{II}-\mathrm{C}, \mathrm{III}-\mathrm{D}, \mathrm{IV}-\mathrm{A}\) (c) \(\mathrm{I}-\mathrm{E}, \mathrm{II}-\mathrm{C}, \mathrm{III}-\mathrm{D}, \mathrm{IV}-\mathrm{A}\) (d) \(\mathrm{I}-\mathrm{B}, \mathrm{II}-\mathrm{A}, \mathrm{III}-\mathrm{C}, \mathrm{IV}-\mathrm{D}\)

5 step solution

Problem 125

Consider the following compounds: I. DDT II. gammexane III. carbon tetrachloride IV. chlorobenzene The correct sequence of these compounds in the increasing order of percentage of chlorine in them is (a) I, II, III, IV (b) IV, I, II, III (c) IV, II, I, III (d) III, I, II, IV

5 step solution

Problem 126

Consider the following haloalkanes: 1\. \(\mathrm{CH}_{3} \mathrm{~F}\) 2\. \(\mathrm{CH}_{3} \mathrm{Cl}\) 3\. \(\mathrm{CH}_{3} \mathrm{Br}\) 4\. \(\mathrm{CH}_{3} \mathrm{I}\) The increasing order of reactivity in nucleophilic substitution reaction is (a) \(4<3<2<1\) (b) \(1<3<2<4\) (c) \(1<2<3<4\) (d) \(1<2<4<3\)

4 step solution

Problem 127

Which of the following will give a positive carbylamine test? 1\. \(\mathrm{H}_{3} \mathrm{C}-\mathrm{NH}_{2}\) 2\. \(\mathrm{H}_{3} \mathrm{C}-\mathrm{NH}-\mathrm{CH}_{3}\) 3\. \(\left(\mathrm{CH}_{3}\right)_{3} \mathrm{~N}\) 4\. \(\mathrm{C}_{6} \mathrm{H}_{5}-\mathrm{NH}_{2}\) Select the correct answer using the codes given below. (a) 1 and 3 (b) 2 and 4 (c) 1 and 4 (d) 3 and 4

7 step solution

Problem 128

Identify the set of reagents/reaction conditions 'X' and ' \(\mathrm{Y}\) ' in the following set of transformations: CCCBr (a) \(\mathrm{X}=\) dilute aqueous \(\mathrm{NaOH}, 20^{\circ} \mathrm{C}\) \(\mathrm{Y}=\) HBr/acetic acid, \(20^{\circ} \mathrm{C}\) (b) \(\mathrm{X}=\) concentrated alcoholic \(\mathrm{NaOH}, 80^{\circ} \mathrm{C}\) \(\mathrm{Y}=\mathrm{HBr} /\) acetic acid, \(20^{\circ} \mathrm{C}\) (c) \(\mathrm{X}=\) dilute aqueous \(\mathrm{NaOH}, 20^{\circ} \mathrm{C}\) \(\mathrm{Y}=\mathrm{Br}_{2} / \mathrm{CHCl}_{3}, 0^{\circ} \mathrm{C}\) (d) \(\mathrm{X}=\) concentrated alcoholic \(\mathrm{NaOH}, 80^{\circ} \mathrm{C}\) \(\mathrm{Y}=\mathrm{Br}_{2} / \mathrm{CHCl}_{3}, 0^{\circ} \mathrm{C}\)

4 step solution

Problem 129

Toluene when treated with \(\mathrm{Br}_{2}\) and \(\mathrm{Fe}\), gives \(\mathrm{p}\)-bromotoluene as the major product, because the methyl group 1\. is para-directing 2\. is m-directing 3\. activates the ring by hyperconjugation 4\. deactivates the ring of the above (a) 1,3 (b) \(1,2,3\) (c) 1,2 (d) none of these

5 step solution

Problem 131

Aryl halides are less reactive towards nucleophilic substitution reactions as compared to alkyl halides due to 1\. the formation of less stable carbonium ion 2\. resonance stabilization 3\. longer carbon-halogen bond 4\. the inductive effect 5\. sp \(^{2}\) hybridized carbon attached to halogen (a) \(1,2,3\) (b) \(2,4,5\) (c) 2,5 (d) 4,5

5 step solution

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