Aldehydes, Keto...

Only One Option Correct Type

Direction (Q. Nos. 1-12) This section contains 12 multiple choice questions. Each question has four choices (a), (b), (c) and (d), out of which ONLY ONE is correct.

Q. 

An optically active organic compound has molecular formula C₅H₁₂O(X). X on oxidation with CrO₃/H₂SO₄ gives an achiral C₅H₁₀O. Hence, X could be

Which of the following reaction will not produce an aldehyde?

Which reagent below cannot reduce an acid chloride to an aldehyde?

The incorrect statement regarding oxo process for synthesis of an aldehyde is

All of the following reaction gives atleast one ketone as a significant organic product except

All of the following results in the formation of an aldehyde except

Consider the following reaction,

All of the following reagents can bring about the above transformation except

A hydrocarbon X(C₇H₁₂) on ozonolysis followed by the treatment with (CH₃)₂S gives C₇H₁₂O₂ which gives positive Tollen’s test as well as positive iodoform test. The compoppd below satisfying the criteria of X is

A hydrocarbon X has molecular formula C₅H₁₀ X on treatment with B₂H₆ in H₂O₂ /NaOH gives an optically active C₅H₁₂O which on treatment with CrO₃/HCI / pyridine gives C₅H₁₀O which is still chiral. Which of the following can be a product of reductive ozonolysis of X?

What is the final major product of the following reaction

Consider the following reaction,

(A pure enantiomer)

Q. 

The incorrect statement regarding X is

Consider the following reaction sequence,

Q. 

The correct statement regarding X is