organic chem

i know the answer. so please give the steps.

3 Answers

1
Athenes Analyst ·

In Q1)

STEP 1: OH- would cleave due to H2SO4 leaving a positive charge on carbon. Then there would be RING expansion forming CYCLOHEXENE

STEP 2: With NBS at 2 carbons next to double bonded carbon Br- would substitute at place of hydrogen.

STEP 3: With alc KOH which is a dehalogenating agent form BENZENE

1
Athenes Analyst ·

Q2) Friedel Crafts

1
Abhinav Gupta ·

I think cyclopentane will be formed in step 1in Q1

Your Answer

Close [X]