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