Step 1: Friedlander's Synthesis. Friedlander's synthesis is the reaction of o-aminobenzaldehyde with an electrophilic reagent, corresponding to (I) o-Aminobenzaldehyde.
Step 2: Doebner-Miller's Synthesis. Doebner-Miller's synthesis is the reaction of $\beta$-phenylethylamide with an electrophile, corresponding to (II) $\beta$-Phenylethylamide.
Step 3: Hantzsch's Synthesis. Hantzsch's synthesis is the reaction of aniline with a carbonyl compound, corresponding to (III) Aniline.
Step 4: Bischler-Napieralski's Synthesis. Bischler-Napieralski's synthesis is the reaction of a $\beta$-ketoneester with an amine, corresponding to (IV) $\beta$-Ketoneester.
Step 5: Conclusion. The correct matching is (A) - (I), (B) - (II), (C) - (III), (D) - (IV), which is option (1).
Final Answer: \[ \boxed{\text{(1) (A) - (I), (B) - (II), (C) - (III), (D) - (IV)}} \]
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:
