Which of the following structures most closely represents an intermediate in the electrophilic bromination of para-xylene?
Correct answer: C. Option C
- A. Option A
- B. Option B
- C. Option C
- D. Option D
Explanation
As in the bromination of para-xylene bromine cation attacks on xylene ring at the ortho position and forms the intermediate.
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
The reaction of isobutane with an unknown halogen is catalyzed by light. Identify the halogen if the two major products seen in a white mixture, obtained are:
Ethylamine can be prepared by the action of bromine and caustic potash on:
Elimination from 2 - bromobutane results in:
SN2 reactions can be best carried out with:
Which one of the following is NOT a nucleophile?
In general formula of alkyl halide RX, X represents _