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

Show how the following compound can be converted to benzoic acid. Acetophenone - Chemistry

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प्रश्न

Show how the following compound can be converted to benzoic acid.

Acetophenone

रासायनिक समीकरणे/रचना

उत्तर

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पाठ 12: Aldehydes, Ketones and Carboxylic Acids - Intext Questions [पृष्ठ ३७०]

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एनसीईआरटी Chemistry [English] Class 12
पाठ 12 Aldehydes, Ketones and Carboxylic Acids
Intext Questions | Q 7.2 | पृष्ठ ३७०

संबंधित प्रश्‍न

How is carbolic acid prepared from chlorobenzene?


Predict the products of the following reactions:


Show how the following compound can be converted to benzoic acid.

Phenylethene (Styrene)


An organic compound (A) (molecular formula C8H16O2) was hydrolysed with dilute sulphuric acid to give a carboxylic acid (B) and an alcohol (C). Oxidation of (C) with chromic acid produced (B). (C) on dehydration gives but-1-ene. Write equations for the reactions involved.


How will you prepare the given compound from benzene? You may use any inorganic reagent and any organic reagent having not more than one carbon atom.

Methyl benzoate


How will you prepare the given compound from benzene? You may use any inorganic reagent and any organic reagent having not more than one carbon atom.

p-Nitrobenzoic acid


How is methoxy benzene prepared from carbolic acid?


Name the reagents used in the following reactions:


The functional group present in triacylglycerol is _______.


The reagent which does not react with both, acetone and benzaldehyde.


Match the reactions given in Column I with the suitable reagents given in Column II.

Column I
(Reactions)
Column II
(Reagents)
(i) Benzophenone Diphenylmethane (a) \[\ce{LiAlH4}\]
(ii) Benzaldehyde 1-Phenylethanol (b) \[\ce{DIBAL-H}\]
(iii) Cyclohexanone Cyclohexanol (c) \[\ce{Zn(Hg)/Conc. HCl}\]
(iv) Phenyl benzoate Benzaldehyde (d) \[\ce{CH3MgBr}\]

Assertion: Aldehydes and ketones, both react with Tollen’s reagent to form silver mirror.

Reason: Both, aldehydes and ketones contain a carbonyl group.


The end product Y in the sequence of reaction:

\[\ce{RX ->[CN^-] X ->[NaOH] Y}\] is:


Alkaline hydrolysis of C4H8Cl2 gives a compound (A) which on heating with NaOH and I2 produces a yellow precipitate of CHI3. The compound (A) should be ______.


Hex-4-ene-2-ol on treatment with PCC gives 'A'. 'A' on reaction with sodium hypoiodite gives 'B', which on further heating with soda lime gives 'C. The compound 'C' is ______.


Fill in the blanks by choosing the appropriate words from those given in the brackets:

[stable, low, aldehyde, unstable, 6, 4, ethane, Clemmensen’s, 2, 3, carboxylic acid, high, propane, Rosenmund's]

The primary alcohols are easily oxidised first into ______ and then into ______.


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