Step 1: Base Catalysis.
The Benzil-Benzylic acid rearrangement and Cannizzaro reaction are both base-catalyzed. A base deprotonates the intermediate in the Benzil-Benzylic acid rearrangement. Hydroxide ions facilitate hydride transfer in the Cannizzaro reaction.
Step 2: Anion Shifting.
Anion shifting occurs in the mechanisms of both reactions. In the Benzil-Benzylic acid rearrangement, an anion forms during intermediate creation. The Cannizzaro reaction involves an aldehyde anion in hydride transfer.
Step 3: Inter- and Intra-molecular Reactions.
Both reactions can proceed via inter-molecular and intra-molecular pathways. However, this characteristic is not universally applicable to all instances of both reactions. Therefore, statement (C) is not definitively true for both.
Step 4: Redox Reactions.
Both reactions involve redox changes. The Cannizzaro reaction features one molecule undergoing reduction and another oxidation. The Benzil-Benzylic acid rearrangement also encompasses a redox process.
Step 5: Conclusion.
Consequently, the correct option is (2), encompassing statements (A), (B), and (D) exclusively.
Final Answer: \[\boxed{\text{(2) (A), (B) and (D) only}}\]
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 reaction is carried out by:
