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प्रश्न
What happens when ethanal is treated with excess ethanol and acid?
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उत्तर
When ethanal reacts with excess ethanol and acid gives acetal.
\[\begin{array}{cc}
\phantom{.......}\ce{CH3}\phantom{.........................}\ce{CH3}\phantom{....}\ce{OC2H5}\\
\phantom{....}\backslash\phantom{..........................}\backslash\phantom{..}/\\
\ce{= O + \underset{(excess)}{C2H5OH} ->[H^⊕]}\\
\phantom{....}/\phantom{..........................}/\phantom{..}\backslash\\
\phantom{.........}\ce{H}\phantom{.........................}\ce{H}\phantom{.....}\ce{OC2H5}\\
\end{array}\]
APPEARS IN
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
Draw the structure of the semicarbazone of ethanal.
What is meant by the following term? Give an example of the reaction in the following case.
Schiff’s base
Acetaldehyde, Acetone, Di-tert-butyl ketone, Methyl tert-butyl ketone (reactivity towards HCN)
Write the main product formed when propanal reacts with the following reagents:
2 moles of 3 CH OH in presence of dry HCl
Paraldehyde is formed as a result of polymerisation:-
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 hexane-3-one
Draw structures of the following derivative.
The ethylene ketal of hexan-3-one
The product of the following reaction is
\[\begin{array}{cc}
\ce{O}\phantom{.........}\\
||\phantom{.........}\\
\ce{C2H5 - C - CH3 ->[H2/Ni][\Delta] \phantom{..}?}\end{array}\]
