Step 1: Base Catalysis.
Both the Benzil-Benzylic acid rearrangement and Cannizzaro's reaction are base-catalyzed reactions. In the Benzil-Benzylic acid rearrangement, the base is required to deprotonate the intermediate. Similarly, in Cannizzaro's reaction, hydroxide ions facilitate the transfer of hydride.
Step 2: Anion Shifting.
Both reactions involve the shifting of an anion in their mechanisms. In the Benzil-Benzylic acid rearrangement, an anion is formed during the formation of the intermediate, and in the Cannizzaro reaction, an anion of the aldehyde is involved in the hydride transfer.
Step 3: Inter and Intra-molecular Reactions.
Both reactions can occur inter-molecularly and intra-molecularly. However, this is not specifically true for both reactions and doesn't apply to all cases. Thus, (C) is not necessarily true for both reactions.
Step 4: Redox Reactions.
Both reactions involve redox changes. In the Cannizzaro reaction, one molecule undergoes reduction while another undergoes oxidation. The Benzil-Benzylic acid rearrangement also involves a redox process.
Step 5: Conclusion.
Thus, the correct answer is (2) (A), (B) and (D) only.
Final Answer: \[ \boxed{\text{(2) (A), (B) and (D) only}} \]
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:
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: