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कर्नाटक बोर्ड पी.यू.सी.पीयूसी विज्ञान 2nd PUC Class 12

Write a test to differentiate between pentan-2-one and pentan-3-one.

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प्रश्न

Write a test to differentiate between pentan-2-one and pentan-3-one.

टीपा लिहा
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उत्तर

Pentan--one having a group forms a yellow ppt. of iodoform with an alkaline solution of iodine (i.e., iodoform test) while pentan-3-one does not.

\[\begin{array}{cc}
\ce{O}\phantom{.....................................}\\
||\phantom{.....................................}\\
\ce{CH3CH2\underset{Pentan-2-one}{CH2 - C - CH3} ->[I2/NaOH][(Iodoform test)] \underset{Yellow ppt.}{CHI3} + \underset{Sodium butanoate}{CH3CH2CH2COONa}}
\end{array}\]

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पाठ 12: Aldehydes, Ketones and Carboxylic Acids - Multiple Choice Questions (Type - I) [पृष्ठ १७२]

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एनसीईआरटी एक्झांप्लर Chemistry Exemplar [English] Class 12
पाठ 12 Aldehydes, Ketones and Carboxylic Acids
Multiple Choice Questions (Type - I) | Q 20 | पृष्ठ १७२

संबंधित प्रश्‍न

Arrange the following compound in increasing order of its reactivity in nucleophilic addition reactions.

Ethanal, Propanal, Propanone, Butanone.

Hint: Consider steric effect and electronic effect.


What is meant by the following term? Give an example of the reaction in the following case.

Oxime


How are the following compounds prepared?

acetophenone from benzene


Give a simple chemical test to distinguish between 
 


Write the main product formed when propanal reacts with the following reagents: 
2 moles of 3 CH OH in presence of dry HCl 


The pH of blood does not appreciably change by a small addition of acid or base because


Which one of the following gives only one monochloro derivative?


Which among the following is most reactive to give nucleophilic addition?


The product "P" in the above reaction is:


The increasing order of the following compounds towards HCN addition is:

(i)
(ii)
(iii)
(iv)

Which of the following is most reactive in nucleophilic addition reactions?


The following questions are case-based questions. Read the passage carefully and answer the questions that follow:

The carbon-oxygen double bond is polarised in aldehydes and ketones due to higher electronegativity of oxygen relative to carbon. Therefore, they undergo nucleophilic addition reactions with a number of nucleophiles such as HCN, NaHSO3, alcohols, ammonia derivatives and Grignard reagents. Aldehydes are easily oxidised by mild oxidising agents as compared to ketones. The carbonyl group of carboxylic acid does not give reactions of aldehydes and ketones. Carboxylic acids are considerably more acidic than alcohols and most of simple phenols.

Answer the following:

(a) Write the name of the product when an aldehyde reacts with excess alcohol in the presence of dry HCl. (1)

(b) Why carboxylic acid is a stronger acid than phenol? (1)

(c) (i) Arrange the following compounds in increasing order of their reactivity towards CH3MgBr: (1)

CH3CHO, \[\begin{array}{cc}
\ce{(CH3)3C-C-CH3}\\
\phantom{....}||\\
\phantom{....}\ce{O}
\end{array}\],  \[\begin{array}{cc}
\ce{CH3-C-CH3}\\
||\\
\ce{O}
\end{array}\]

(ii) Write a chemical test to distinguish between propanal and propanone. (1)

OR

(c) Write the main product in the following: (2)

(i)
(ii)

Out of p-tolualdehyde and p-nitrobenzaldehyde, which one is more reactive towards nucleophilic addition reactions, why?


Draw the structure of the following derivative.

The ethylene ketal of hexane-3-one


Draw structures of the following derivatives.

Acetaldehydedimethylacetal


Draw structure of the following derivative.

The ethylene ketal of hexan-3-one


Give an example of the reaction in the following case.

Oxime


Give an example of the reaction in the following case.

Imine


Complete the following reaction:

[C] is __________.


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