The major product (P) in the following transformation is:
Step 1: Borane Reduction.
The reaction starts with diborane (\(B_2H_6\)) and hydrogen peroxide (\(H_2O_2\)) in the presence of NaOH, which reduces the ethoxy group to a hydroxyl group. This results in the formation of a diol at positions 1 and 6 of the hexane chain.
Step 2: Hydrolysis of the Organoborane.
The organoborane intermediate is hydrolyzed to form the desired diol product.
Step 3: Conclusion.
The product formed is Hexane-1,6-diol, making option (1) the correct answer.
Final Answer: \[ \boxed{\text{(1) Hexane-1,6-diol}} \]
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:
Above conversion is carried out using:
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: