Which of the following name reaction used to form Amines through amides?

Correct answer: C. Hoffmannbromamide

  • A. cannizaro
  • B. Claisen
  • C. Hoffmannbromamide
  • D. Schmidt

Explanation

The Hofmann-Bromamide reaction is a chemical reaction used to convert primary amides to primary amines. The reaction involves the reaction of a primary amide with bromine in the presence of a strong base, such as sodium or potassium hydroxide, to form an isocyanate intermediate. The isocyanate intermediate then undergoes hydrolysis to form a primary amine.

Written and checked by , M.Phil ChemistryLast updated
Report an error

The more specific you are, the faster it gets fixed. A source beats an opinion.

Prefer email? [email protected]

About Alkyl Halides

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.

Practise Alkyl Halides

458 free Alkyl Halides MCQs from Chemistry, each with the correct answer and an explanation. Unlimited attempts, no account needed.

Discussion

Stuck on an option, or know a faster way to get there? Ask or explain it here.

No comments yet. Be the first to explain this one.

Exams that ask Chemistry questions like this

Chemistry is on 14 papers prepared for on TestUstad, and all of them draw the same bank, so this question is worth knowing for every one of them.

More Alkyl Halides questions