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

Predict the products formed when cyclohexanecarbaldehyde reacts with the following reagents. Semicarbazide and weak acid

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प्रश्न

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

Semicarbazide and weak acid

रासायनिक समीकरणे/रचना
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उत्तर

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पाठ 8: Aldehydes, Ketones and Carboxylic Acids - Exercises [पृष्ठ २५६]

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एनसीईआरटी Chemistry Part 1 and 2 [English] Class 12
पाठ 8 Aldehydes, Ketones and Carboxylic Acids
Exercises | Q 8.6 (iii) | पृष्ठ २५६

संबंधित प्रश्‍न

Acetaldehyde, when treated with which among the following reagents does NOT undergo addition reaction?

(A) Ammonia

(B) Hydroxylamine

(C) Ammoniacal silver nitrate

(D) Semicarbazide


Write balanced chemical equations for action of ammonia on - formaldehyde


How are the following compounds prepared?

benzaldehyde from benzene


Write the products formed when CH3CHO reacts with the following reagents : HCN

 


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

Cyanohydrin


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

Hemiacetal


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


What is the action of the following reagents on ethanoic acid?

1) `LiAlH_4"/"H_3O^+`

2) `PCl_3 , "heat"`

3) `P_2O_5, "heat"`


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


Identify the compounds A, B and C in the following reaction.

\[\ce{CH3 - Br ->[Mg/ether] (A) ->[(i) CO][(ii) Water] (B) ->[CH3OH/H+][Δ] (C)}\]


Write the name of product formed, when acetone is treated with 2, 4-dinitrophenyl hydrazine.


The product "P" in the above reaction is:


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)

Write the structure of the product formed when acetone reacts with 2, 4 DNP reagent.


Draw structure of the following derivative.

Acetaldehydedimethylacetal


Draw structure of the following derivative.

The ethylene ketal of hexan-3-one


Draw the 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 structures of the given derivatives.

The ethylene ketal of hexan-3-one


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