The major product (P) in the following transformation is:

Step 1: Borane Reduction. The reaction begins with diborane (\(B_2H_6\)) and hydrogen peroxide (\(H_2O_2\)) in the presence of NaOH. This mixture converts the ethoxy group to a hydroxyl group, producing a diol at positions 1 and 6 of the hexane chain.
Step 2: Hydrolysis of the Organoborane. The organoborane intermediate undergoes hydrolysis to yield the target diol product.
Step 3: Conclusion. The resulting product is Hexane-1,6-diol. Therefore, option (1) is the correct answer.
Final Answer: \[ \boxed{\text{(1) Hexane-1,6-diol}} \]
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:

Above conversion is carried out using:
The reaction is carried out by:
