
Above conversion is carried out using:
Step 1: KOH (alc.). Potassium hydroxide in alcohol (KOH (alc.)) causes elimination of the bromine atom, resulting in the formation of an alkene.
Step 2: Oxymurcuration-demercuration. The alkene subsequently undergoes oxymurcuration-demercuration, yielding an alcohol at the original site of bromine attachment. Therefore, option (1) is correct.
Final Answer: \[ \boxed{\text{(1) (I) KOH (alc.), (II) oxymurcuration-demercuration}} \]
Which of the following amino compound(s) CANNOT be prepared by Gabriel phthalimide synthesis?
(A) n-Butylamine
(B) Alanine
(C) Aniline
(D) t-Butylamine
Choose the correct answer from the options given below:
The major product (P) in the following transformation is:

The reaction is carried out by:
