Acetaldyde on warming with Tollen’s reagent gives a bright mirror in the inner sides of the test tube.The bright mirror is due to deposition of ………………….

Acetaldyde on warming with Tollen’s reagent gives a bright mirror in the inner sides of the test tube.What is Tollen’s reagent ?

Acetaldyde on warming with Tollen’s reagent gives a bright mirror in the inner sides of the test tube.Can you do the above experiment using Ketones?

C_3 H_6 O did not give a silver mirror with Tollens’ reagent, but gave an oxime with hydroxylamine. It can give positive iodoform test Fehling's test Schiff's test Carbylamine test

Structure of C_8H_8Cl_2 , which on treatment with aqueous alkali followed by dehydration gives a product which does not give positive iodoform test, but gives silver mirror test, is:

The compound C_4 H_8 Cl_2 (A) an hydrolysis gives a compound C_4 H_8 O_1(B) . The compound (B) reacts with hydroxylamine and gives a negative test with Tollen's reagent. What are (A)and (B), Support your answer with proper reasoning and give the equations of reactions.

An organic compound cọntains 69.77 %carbon, 11.63 % hydrogen and rest oxygen. The molecular mass of the compound is 86 . It does not reduce Tollens' reagent but forms an addition compound with sodiumhydrogensulphite and give positive iodoform test. On vigorous oxidation it gives ethanoic and propanoicacid. Write the possible structure of the compound.

A research scholar retumed to the laboratory after the lock down due to Covid-19. He kept acetone, benzaldehyde, acetaldehyde and diethyl ketone irl four different bottles. The bottles cortained only the label as p, e, i and S. He forgot which bottle contained which compound. Compounds p and _R orry underwent iodoform test. Compound R alone gave reddish brown piecipitate with Fehling,s reagent. Compounds Q and R alone underwent Tollen,s test. Compound S did not ans*er any ofthe above tests. Identiry the compounds P, Q, rt and S.