Above conversion is carried out using:
Step 1: KOH (alc.).
Potassium hydroxide in alcohol (KOH (alc.)) induces elimination of the bromine atom, producing an alkene.
Step 2: Oxymurcuration-demercuration.
The alkene then undergoes oxymurcuration-demercuration to form an alcohol at the position where the bromine was originally attached. Hence, option (1) is correct.
Final Answer: \[ \boxed{\text{(1) (I) KOH (alc.), (II) oxymurcuration-demercuration}} \]
The reaction is carried out by:
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 final product (D) in the above sequential reaction is:
The major product (P) in the following transformation is:
Match List-I with List-II and choose the correct answer:
Match List-I with List-II:
Who said this sentence –
Match List-I with List-II and choose the correct answer:
Match List-I with List-II and choose the correct answer: