Free Nucleophilic Addition Reactions MCQs with Answers

35 Nucleophilic Addition Reactions MCQs from Chemistry, each with the correct answer and a written explanation of why it is correct. Free and unlimited, with no account needed.

Nucleophilic addition occurs at the polar carbonyl group of aldehydes and ketones, where a nucleophile attacks the electron-deficient carbon atom. Reactions with hydrogen cyanide, sodium bisulfite, alcohols and Grignard reagents are explained through tetrahedral intermediates, acid or base catalysis, and the different reactivity of aldehydes and ketones.

Last updated

35 questions · page 2 of 2

  • A. Acid.
  • B. Base.
  • C. Water.
  • D. Both acid and base.

Explanation: Nucleophilic addition reactions of carbonyl compounds involve the addition of a nucleophile (an electron-rich species) to the carbon atom…

Correct answer: Both acid and base.
  • A. Elimination+ addition
  • B. Elimination+ Substitution
  • C. Addition + substitution
  • D. None of these

Explanation: Condensation involves elimination and addition. It is a reaction in which a water molecule is produced as a by-product.

Correct answer: Elimination+ addition
  • A. Sulphide ion
  • B. Sulfite ion
  • C. Hydride ion
  • D. Sodium ion

Explanation: The addition of sodium bisulfite to a carbonyl group takes place as follows:Sodium bisulfite ionizes to form sulfite ions.The sulfite ion…

Correct answer: Sulfite ion
  • A. Hydroxyl ion
  • B. Carbocation
  • C. Carbanion
  • D. Water

Explanation: The reaction mechanism below shows that the carbanion is the nucleophile of the reaction:

Correct answer: Carbanion
  • A. Carbanion
  • B. Carbocation
  • C. Carbene
  • D. Alkoxide ion

Explanation: During the reduction of aldehydes with NaBH4, the "alkoxide ion" is seen as the intermediate formed hence the answer is D.

Correct answer: Alkoxide ion
  • A. Propane
  • B. Butane
  • C. Methane
  • D. Ethane

Explanation: Explanation:The reaction is a typical Grignard reagent hydrolysis reaction where the Grignard reagent (CH3CH2MgBr) reacts with water to…

Correct answer: Ethane
  • A. Nucleophilic addition
  • B. Electrophilic addition
  • C. Electrophilic substitution
  • D. Nucleophilic substitution

Explanation: It is an example of nucleophilic addition. The CN- ion has a negative charge and it is attracted to a positive charge so CN- is a…

Correct answer: Nucleophilic addition
  • A. Nucleophilic addition
  • B. Nucleophilic substitution
  • C. Electrophilic addition
  • D. Addition elimination

Explanation: This reaction is called an addition-elimination reaction since a water molecule is eliminated from the reaction whereas the lone pair of…

Correct answer: Addition elimination
  • A. CH3OH
  • B. C2H5OH
  • C. (CH3)2CHOH
  • D. ....

Explanation: When a Grignard reagent reacts with aldehydes and ketones, it results in production of addition products which on hydrolysis gives…

Correct answer: C2H5OH
  • A. Alcohol and aldehyde functional groups
  • B. Alcohol and ether functional groups
  • C. Aldehyde and ether functional groups
  • D. Alcohol and carboxylic acid functional groups

Explanation: Hemiacetal is a molecule made up of a core carbon atom connected to four groups: -OR, -OH, -R, and -H.

Correct answer: Alcohol and ether functional groups
  • A. CH3CH2OH
  • B. CH3CH2CHO
  • C. CH3CH(OH)CH2CH3
  • D. CH3CH2CH2OH

Explanation: The correct answer is CH3CH(OH)CH2CH3. In this Grignard reaction, the ethyl group from the Grignard reagent (CH3CH2MgBr) adds to the…

Correct answer: CH3CH(OH)CH2CH3
  • A. A compound formed by the reaction of an aldehyde with hydrazine.
  • B. A compound formed by the reaction of an aldehyde with water.
  • C. A compound formed by the reaction of an aldehyde with an amine.
  • D. A compound formed by the reaction of an aldehyde with hydrogen cyanide.

Explanation: Aldehyde hydrazones are organic compounds derived from the reaction of aldehydes with hydrazine (NH2-NH2) or its derivatives.

Correct answer: A compound formed by the reaction of an aldehyde with hydrazine.
  • A. Electrophilic addition reaction
  • B. Substitution reaction
  • C. Nucleophilic addition reaction
  • D. None of these

Explanation: So, when aldehydes undergo nucleophilic addition reactions, it means that a nucleophile (a species with a lone pair of electrons) attacks…

Correct answer: Nucleophilic addition reaction
  • A. Aldehyde
  • B. Ketone
  • C. Acid halide
  • D. Carboxylic acid

Explanation: Grignard's reagent (RMgX) reacts with ketones to produce tertiary alcohols.

Correct answer: Ketone
  • A. To act as strong acid
  • B. To act as nucleophile and add to carbonyl compounds
  • C. To act as electrophile
  • D. To catalyze hydrogenation reaction

Explanation: Grignard reagents are highly reactive nucleophiles that add to carbonyl compounds such as aldehydes and ketones to form addition products.

Correct answer: To act as nucleophile and add to carbonyl compounds