Advertisements
Advertisements
Question
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
Advertisements
Solution

APPEARS IN
RELATED QUESTIONS
On acid hydrolysis, propane nitrile gives.
How is carbolic acid prepared from chlorobenzene?
Identify ‘A' and ‘B’ in the following reaction :
C6H5MgBr + C02 `(`> ‘A’ `(PCl_5)/()`> ‘B’
Show how the following compound can be converted to benzoic acid.
Phenylethene (Styrene)
Predict the products formed when cyclohexanecarbaldehyde reacts with the following reagent.
Tollens’ reagent
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
Complete the synthesis by giving missing starting material, reagent or product.

The functional group present in triacylglycerol is _______.
The reagent which does not react with both, acetone and benzaldehyde.
Which is the most suitable reagent for the following conversion?
\[\begin{array}{cc}
\phantom{....................}\ce{O}\phantom{.....................................}\ce{O}\phantom{.}\\
\phantom{....................}||\phantom{......................................}||\phantom{.}\\
\phantom{}\ce{CH3 - CH = CH - CH2 - C - CH3 -> CH3 - CH = CH - CH2 - C - OH}\phantom{.}
\end{array}\]
Through which of the following reactions number of carbon atoms can be increased in the chain?
(i) Grignard reaction
(ii) Cannizaro’s reaction
(iii) Aldol condensation
(iv) HVZ reaction
Which of the following substance produced acetaldehyde on dry distillation?
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.
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 ______.
\[\ce{->[CO,HCl][Anhyd. AlCl3/CuCl]}\]