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Haloalkanes and Haloarenes

NEET (UG) 2022 (Phase 2)MCQMedium📈 Topic in 12% papers+4−1
Ques. 1NEET (UG) 2022 (Phase 2)

Given below are two statements : one is labelled as Assertion (A) and the other is labelled as Reason (R). In the light of the above statements, choose the most appropriate answer from the options given below :

  1. (A) is not correct but (R) is correct
  2. Both (A) and (R) are correct and (R) is the correct explanation of (A)
  3. Both (A) and (R) are correct but (R) is not the correct explanation of (A)
  4. (A) is correct but (R) is not correct

Answer

(4) (A) is correct but (R) is not correct

Solution

As per NCERT, chlorine withdraws electrons through inductive effect and releases electrons through resonance.

Through resonance, electron density increases more at the ortho and para positions, so the halogen is ortho, para directing and Assertion (A) is correct.

Through inductive effect chlorine destabilises the intermediate carbocation, while through resonance the halogen tends to stabilise it, and this effect is more pronounced at the ortho and para positions.

∵ The inductive effect is stronger than the resonance effect and causes net electron withdrawal (deactivation of the ring), the resonance effect is not the more pronounced one.

∴ The statement in Reason (R), that the resonance effect is more pronounced (than the inductive effect), is not correct.

Answer: (4)

Keep practising — Haloalkanes and Haloarenes

Ques. 2NEET (UG) 2022 (Phase 2)

Predict the order of reactivity of the following four isomers towards SN2 reaction. (I) CH3CH2CH2CH2Cl (II) CH3CH2CH(Cl)CH3 (III) (CH3)2CHCH2Cl (IV) (CH3)3CCl

  1. (IV) > (II) > (III) > (I)
  2. (IV) > (III) > (II) > (I)
  3. (I) > (II) > (III) > (IV)
  4. (I) > (III) > (II) > (IV)
Ques. 3NEET (UG) 2021

The major product formed in dehydrohalogenation reaction of 2-bromopentane is pent-2-ene. This product formation is based on?

  1. Hückel's Rule
  2. Saytzeff's Rule
  3. Hund's Rule
  4. Hofmann Rule
Ques. 4NEET (UG) 2021

The correct sequence of bond enthalpy of 'C-X' bond is :

  1. CH3-Cl > CH3-F > CH3-Br > CH3-I
  2. CH3-F < CH3-Cl < CH3-Br < CH3-I
  3. CH3-F > CH3-Cl > CH3-Br > CH3-I
  4. CH3-F < CH3-Cl > CH3-Br > CH3-I
Ques. 5NEET (UG) 2020

Elimination reaction of 2-Bromopentane to form pent-2-ene is :

  1. A, C and D only
  2. B, C and D only
  3. A, B and D only
  4. A, B and C only
Ques. 6NEET 2018

The compound C7H8 undergoes the following reactions : C7H8 3Cl2/ A Br2/Fe B Zn/HCl C The product 'C' is

  1. m-bromotoluene
  2. o-bromotoluene
  3. 3-bromo-2,4,6-trichlorotoluene
  4. p-bromotoluene
Ques. 7NEET 2017

Identify A and predict the type of reaction. [figure]

  1. [figure] and elimination addition reaction
  2. [figure] and cine substitution reaction
  3. [figure] and cine substitution
  4. [figure] and substitution reaction
Ques. 8NEET 2016 (Phase 2)

Consider the reaction, CH3CH2CH2Br + NaCN CH3CH2CH2CN + NaBr The reaction will be the fastest in

  1. ethanol
  2. methanol
  3. N,N-dimethylformamide (DMF)
  4. water
Ques. 9AIPMT 2015

Which of the following reaction(s) can be used for the preparation of alkyl halides? (I) CH3CH2OH + HCl Anh. ZnCl2 (II) CH3CH2OH + HCl Anh. ZnCl2 (III) (CH3)3COH + HCl Anh. ZnCl2 (IV) (CH3)2CHOH + HCl Anh. ZnCl2

  1. (I) and (II) only
  2. (IV) only
  3. (III) and (IV) only
  4. (I), (III) and (IV) only
Ques. 10AIPMT 2012 (Mains)

In the replacement reaction [figure] The reaction will be most favourable if M happens to be

  1. Na
  2. K
  3. Rb
  4. Li
Ques. 11AIPMT 2011 (Mains)

Which of the following compounds undergoes nucleophilic substitution reaction most easily?

  1. [figure]
  2. [figure]
  3. [figure]
  4. [figure]

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