Free Alkyl Halides MCQs with Answers

458 Alkyl Halides MCQs from Chemistry, each with the correct answer and a written explanation of why it is correct. Free and unlimited, with no account needed.

Alkyl halides are named and related to their carbon-halogen structure, polarity and reactivity. The key reactions are nucleophilic substitution by SN1 and SN2 mechanisms and elimination by E1 and E2 mechanisms, including how substrate structure, nucleophile, base, solvent and temperature influence substitution versus elimination.

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458 questions · page 17 of 23

  • A. It is colourless liquid
  • B. It is used as industrial solvent
  • C. It is insoluble in water and soluble in alcohol for fat, oil etc
  • D. It is inflammable

Explanation: CCl4 is not flammable because the carbon-chlorine bonds are very strong.

Correct answer: It is inflammable
  • A. Electrophilic addition reaction
  • B. β-elimination
  • C. Nucleophilic addition reaction
  • D. Nucleophilic substitution reaction

Explanation: The reaction of a Grignard reagent with methanal (formaldehyde) followed by hydrolysis is a nucleophilic addition reaction.

Correct answer: Nucleophilic addition reaction
  • A. R - X
  • B. Option B
  • C. R - CH2 - X
  • D. Option D

Explanation: Tertiary alkyl halides are the most reactive in SN1 reactions because they have the most stable carbocation intermediates.

Correct answer: Option B
  • A. They have an electrophilic carbon
  • B. They have an electrophilic carbon and a good leaving group
  • C. They have an electrophilic carbon and bad leaving groups
  • D. They have a nucleophilic carbon and a good leaving groups

Explanation: Alkyl halides are considered to be very reactive compounds towards nucleophiles because they have an electrophilic carbon and a good…

Correct answer: They have an electrophilic carbon and a good leaving group
  • A. Option A
  • B. Option B
  • C. Option C
  • D. Option D

Explanation: The chemical formula of halothane is C2H3BrClF3. It is a trihalogenated methane, which means that it has three halogen atoms (bromine…

Correct answer: Option B
  • A. It is used as an anesthetic substance
  • B. It is used as a solvent for fats waxes and resins
  • C. It is used in manufacturing freons
  • D. It is used as preservative for anatomical specimen

Explanation: Chloroform is not used in manufacturing freons. Therefore, option c is correct.

Correct answer: It is used in manufacturing freons
  • A. It is valuable plastic which resists the action of acid and alkali
  • B. It is used as coating the electrical wiring
  • C. It is used as a non-stick coating for cooking pans
  • D. It reacts with oxidants

Explanation: The correct answer to the question "All of the following are characteristic features of Teflon plastic EXCEPT:" is option D: It acts with…

Correct answer: It reacts with oxidants
  • A. Aerosol spray
  • B. Use of chlorofluorocarbons
  • C. Effect of SO2 and NO2 Pollutant
  • D. Global warming by CO2

Explanation: Chlorofluorocarbons breaks ozone molecules by releasing chlorine free radicals.

Correct answer: Use of chlorofluorocarbons
  • A. Reaction of alkyl halide with aqueous KOH
  • B. Reaction of alkyl halide with alcoholic KOH
  • C. Reaction of alkyl halide with KCN followed by acidic hydrolysis
  • D. Reactions of alkyl halide with sodium alkoxide

Explanation: The correct option for the production of alcohol is B. In the reaction of alkyl halide with alcoholic KOH (option B), an elimination…

Correct answer: Reaction of alkyl halide with alcoholic KOH
  • A. 1-Bromo-2-methylbutane
  • B. 4-Bromo-3-methylbutane
  • C. 4-Bromo-2-methylbutane
  • D. 1-Bromo-3-mehtylbutane

Explanation: When applying IUPAC rules:1. Longest continuous carbon chain: There is a four-carbon chain (butane).2.

Correct answer: 1-Bromo-2-methylbutane
  • A. The molecule which undergoes nucleophilic substitution reaction is called substrate
  • B. The group or species which leaves the substrate is called leaving group (nucleofuge)
  • C. Both A and B
  • D. Neither A nor B

Explanation: C is correct because both statements A and B are accurate descriptions in the context of nucleophilic substitution reactions.A.

Correct answer: Both A and B
  • A. (CH3)3C-CH2
  • B. (CH3)3C
  • C. CH3CH2CH2
  • D. CH3CH CH2CH3

Explanation: The most stable carbocation is the one that has the most alkyl groups attached to it.

Correct answer: (CH3)3C
  • A. Neither may be polymerized
  • B. Neither reacts with bromine to give 1,4-Dibromobutane
  • C. Neither reacts with hydrogen to form butane
  • D. Neither exhibits cis-trans isomerism

Explanation: Cis-trans isomerism, also known as geometric isomerism, occurs in alkenes when there is restricted rotation around the carbon-carbon…

Correct answer: Neither exhibits cis-trans isomerism
  • A. I only
  • B. II only
  • C. IIl and IV only
  • D. I, II, III and IV

Explanation: All of the given points are correct in order to differentiate between SN1 and SN2 reaction. Therefore, option d is correct.

Correct answer: I, II, III and IV
  • A. C2H5Br
  • B. C2H5F
  • C. C2H5I
  • D. C2H5Cl

Explanation: Among the options provided, C2H5I (ethyl iodide) is generally more reactive.

Correct answer: C2H5I
  • A. Nucleophiles
  • B. Bases
  • C. Electrophiles
  • D. All of these

Explanation: Electron-deficient species are classified as electrophiles. Electrophiles are species that have a deficiency or partial positive charge of…

Correct answer: Electrophiles
  • A. Carbonium ion
  • B. Oxonium ion
  • C. Carbon ion
  • D. Carbonion

Explanation: The correct answer is A. Carbonium ion. This ion is a carbon atom carrying a positive charge and bonded to three other atoms or groups.

Correct answer: Carbonium ion