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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. PhMgBr and then H3O+ - Chemistry

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प्रश्न

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

PhMgBr and then H3O+

रासायनिक समीकरण/संरचनाएँ
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उत्तर

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

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

संबंधित प्रश्न

How are the following compounds prepared?

benzaldehyde from benzene


Predict the products of the following reactions:

 


Predict the product of the following reaction:


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

Acetal


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


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

\[\ce{C6H5CHO ->[H2NCONHNH2]}\]


Write balanced chemical equations for action of ammonia on - acetone


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"`


What are amines?


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


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.

The ethylene ketal of hexan-3-one


Draw structure of the following derivative:

Acetaldehydedimethylacetal


Draw structure of the following derivative.

The ethylene ketal of hexan-3-one


Draw structures of the following derivatives.

Acetaldehydedimethylacetal


Draw structure of the following derivative:

Acetaldehydedimethylacetal


Draw structures of the given derivatives.

The ethylene ketal of hexan-3-one


Draw structure of the following derivative.

The ethylene ketal of hexan-3-one 


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