Subject

Chemistry

Class

CBSE Class 12

Pre Boards

Practice to excel and get familiar with the paper pattern and the type of questions. Check you answers with answer keys provided.

Sample Papers

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 Multiple Choice QuestionsShort Answer Type

41.

Which class of drugs is used in sleeping pills?

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42.

Although phenoxide ion has more number of resonating structures than Carboxylate ion, Carboxylic acid is a stronger acid than phenol. Give two reasons.


On losing a proton, carboxylic acids forms carboxylate ion and phenol forms phenoxide ion as follows:

RCOO-Carboxylate ion

 

Phenoxide ion

 

Now, the negative charge is delocalized in both molecules as follows:

The conjugate base of the carboxylic acid has two resonance structures in which negative charge in delocalized over two oxygen atoms (since O is more electronegative than C) which stabilises the carboxylate ion.

On the other hand, in phenoxide ion the charge is delocalized over entire molecule on the less electronegative atom (Carbon), thus resonance of phenoxide is not important in comparison to resonance in carboxylate ion.

Further, in carboxylate ion, the negative charge is effectively delocalized over two oxygen atoms whereas it is less effectively delocalized over one oxygen atom and a less electronegative carbon atom.

Thus, Phenol is less acidic than carboxylic acids. In other words, carboxylic acids are stronger acids than phenol

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43.

Complete the following reactions:

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 Multiple Choice QuestionsLong Answer Type

44.

Rate constant ‘k’ of a reaction varies with temperature ‘T’ according to the equation:

 

where Ea is the activation energy.

When a graph is plotted for   a straight line with a slope of -4250 K is obtained. Calculate ‘Ea’ for the reaction.

(R = 8.314 JK-1 mol-1)

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45.

How will you bring about the following conversions?

 (i) Propanone to propane

(ii) Benzoyl chloride to benzaldehyde

(iii) Ethanal to but-2-enal

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46.

Give simple chemical tests to distinguish between the following pairs of compounds:

(i) Ethanal and Propanal

(ii) Benzoic acid and Phenol

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