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 C 5 H 12 O(X). X on oxidation with CrO 3 /H 2 SO 4 gives an achiral C 5 H 10 O. 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?

Li[{(CH 3 ) 3 CO} 3 AIH] at -80°C

[HAI {CH 2 CH(CH 3 ) 2 } 2 ] at - 80°C

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

Mixture of CO and H 2 is allowed to react with an alkene

Co 2 (CO) 8 may be used as a catalyst

[Co(CO) 4 H] may act as a catalyst

This process can also be used in the same manner for the synthesis of ketone

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

A hydrocarbon X(C 7 H 12 ) on ozonolysis followed by the treatment with (CH 3 ) 2 S gives C 7 H 12 O 2 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 C 5 H 10 X on treatment with B 2 H 6 in H 2 O 2 /NaOH gives an optically active C 5 H 12 O which on treatment with CrO 3 /HCI / pyridine gives C 5 H 10 O which is still chiral. Which of the following can be a product of reductive ozonolysis of X?

Preparation of Aldehydes and Ketones(7 Dec) Free MCQ Practice Test with Solutions

	Daily Test for JEE Preparation 360 tests

	Daily Test for JEE Preparation 360 tests

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