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

Complete the synthesis by giving missing starting material, reagent or product. CHO COOH ->[NaCN/HCl]

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प्रश्न

Complete the synthesis by giving missing starting material, reagent or product.

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पाठ 8: Aldehydes, Ketones and Carboxylic Acids - Exercises [पृष्ठ २५७]

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एनसीईआरटी Chemistry Part 1 and 2 [English] Class 12
पाठ 8 Aldehydes, Ketones and Carboxylic Acids
Exercises | Q 8.17 (vi) | पृष्ठ २५७

संबंधित प्रश्‍न

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

2, 4-DNP-derivative


Predict the products formed when cyclohexanecarbaldehyde reacts with the following reagents.

Excess ethanol and acid


Give plausible explanation for the following:

Cyclohexanone forms cyanohydrin in good yield but 2, 2, 6 trimethylcyclohexanone does not.


 Acetone, Acetaldehyde, Benzaldehyde, Acetophenone – reactivity towards addition of HCN. 


Reaction of aqueous sodium hydroxide on chlorobenzene gives which of the following products?


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


Which of the following has the most acidic hydrogen?


What is the action of sodium hypoiodite on acetone?


What happens when propanone is treated with CH3MgBr and then hydrolysed?


Which will undergo faster nucleophilic addition reaction?

Acetaldehyde or Propanone


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)

Draw structure of the following derivative.

Acetaldehydedimethylacetal


The product of the following reaction is

\[\begin{array}{cc}
\ce{O}\phantom{.........}\\
||\phantom{.........}\\
\ce{C2H5 - C - CH3 ->[H2/Ni][\Delta] \phantom{..}?}\end{array}\]


Draw the structure of the following derivative.

Acetaldehydedimethylacetal


Draw structure of the following derivative.

The ethylene ketal of hexan-3-one


Draw structure of the following derivative.

The ethylene ketal of hexan-3-one 


Draw the structure of the given derivative.

The ethylene ketal of hexan-3-one


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