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Show how the following compound can be converted to benzoic acid. Phenylethene (Styrene) - Chemistry

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प्रश्न

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

Phenylethene (Styrene)

How are the following conversions carried out?

Phenylethene into Benzoic acid

रासायनिक समीकरणे/रचना
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उत्तर १

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उत्तर २

Conversion of phenylethene into benzoic acid:

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पाठ 8: Aldehydes, Ketones and Carboxylic Acids - Intext Questions [पृष्ठ २४८]

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एनसीईआरटी Chemistry Part 1 and 2 [English] Class 12
पाठ 8 Aldehydes, Ketones and Carboxylic Acids
Intext Questions | Q 8.7 (iv) | पृष्ठ २४८

व्हिडिओ ट्यूटोरियलVIEW ALL [2]

संबंधित प्रश्‍न

On acid hydrolysis, propane nitrile gives.


How is carbolic acid prepared from chlorobenzene?


Write the structures of A and B in the following reactions


Name the reagents used in the following reactions:


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

Ethylbenzene


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

Acetophenone


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

Bromobenzene


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

Tollens’ reagent


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.

m-Nitrobenzoic acid


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 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.

Phenylacetic acid


How will you bring about the following conversion in not more than two steps?

Benazaldehyde to α-Hydroxyphenylacetic acid


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


What is the action of following reagents on glucose?
1. Bromine water
2. Hydroxylamine


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


Which is the most suitable reagent for the following conversion?

\[\begin{array}{cc}
\phantom{....................}\ce{O}\phantom{.....................................}\ce{O}\phantom{.}\\
\phantom{....................}||\phantom{......................................}||\phantom{.}\\
\phantom{}\ce{CH3 - CH = CH - CH2 - C - CH3 -> CH3 - CH = CH - CH2 - C - OH}\phantom{.}
\end{array}\]


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.


Substitution of one alkyl group by replacing hydrogen of primary amines


Which of the following substance produced acetaldehyde on dry distillation?


Benzoic acid can be obtained by the oxidation of all of the following EXCEPT ______.


Match List - I with List - II.

List - I List - II
(a) \[\ce{->[CO,HCl][Anhyd. AlCl3/CuCl]}\] (i) Hell-Volhard-Zelinsky reaction
(b)
\[\begin{array}{cc}
\ce{O}\phantom{.................}\\
||\phantom{.................}\\
\ce{R - C - CH3 + NaOX ->}
\end{array}\]
(ii) Gattermann-Koch reaction
(c) \[\ce{R - CH2 - OH + R'COOH ->[Conc. H2SO4]}\] (iii) Haloform reaction
(d) \[\ce{R - CH2COOH ->[(i) X2/Red P][(ii) H2O]}\] (iv) Esterification

Choose the correct answer from the options given below.


Y is:


A compound 'X' with molecular formula C3H8O can be oxidised to a compound 'Y' with the molecular formula C3H6O2 'X' is most likely to 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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