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When liquid ‘A’ is treated with a freshly prepared ammoniacal silver nitrate solution, it gives bright silver mirror. The liquid forms a white crystalline solid on treatment with sodium hydrogensulphi - Chemistry

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प्रश्न

When liquid ‘A’ is treated with a freshly prepared ammoniacal silver nitrate solution, it gives bright silver mirror. The liquid forms a white crystalline solid on treatment with sodium hydrogensulphite. Liquid ‘B’ also forms a white crystalline solid with sodium hydrogensulphite but it does not give test with ammoniacal silver nitrate. Which of the two liquids is aldehyde? Write the chemical equations of these reactions also.

दीर्घउत्तर
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उत्तर

Liquid ‘A’ forms a bright silver mirror on treatment with ammoniacal \[\ce{AgNO3}\] solution, therefore, liquid ‘A’ is an aldehyde.

Liquid B does not give test with ammoniacal \[\ce{AgNO3}\] solution, therefore, liquid ‘B’ must be a methyl ketone.

Chemical equations for these reactions are:

\[\begin{array}{cc}
\phantom{........}\ce{R}\phantom{......................}\ce{R}\phantom{.......}\ce{SO3Na}\phantom{}\\
\phantom{...}\backslash\phantom{......................}\backslash\phantom{...}\phantom{..}/\\\
\phantom{}\ce{C = O + NaHSO3 -> \phantom{..}C}\\
\phantom{.............}/\phantom{......................}/\phantom{.....}\backslash\phantom{..........}\\
\phantom{.....}\ce{\underset{Aldehyde(A)}{H}\phantom{................}\underset{(White crystalline solid)}{\phantom{.}H\phantom{.......}OH}}\phantom{..}
\end{array}\]

\[\begin{array}{cc}
\phantom{........}\ce{R}\phantom{......................}\ce{R}\phantom{.......}\ce{SO3Na}\phantom{}\\
\phantom{...}\backslash\phantom{......................}\backslash\phantom{...}\phantom{..}/\\\
\phantom{}\ce{C = O + NaHSO3 -> \phantom{..}C}\\
\phantom{.............}/\phantom{......................}/\phantom{.....}\backslash\phantom{..........}\\
\phantom{....}\ce{\underset{Methyl ketone (B)}{H3C}\phantom{.............}\underset{(White NaHSO3 adduct)}{\phantom{.}H3C\phantom{.......}OH}}\phantom{.....}
\end{array}\]

\[\ce{\underset{Aldehyde (A)}{R - CHO} + \underset{Tollens reagent}{2[Ag(NH3)2]+} OH- ->[Warm] RCOONH4 + \underset{(Silver mirror)}{2Ag + 3}NH3 + H2O}\]

\[\begin{array}{cc}
\ce{O}\phantom{...............................}\\
||\phantom{...............................}\\
\ce{\underset{Methyl ketone (B)}{R - C - CH3} ->[Tollens reagent] No silver mirror}
\end{array}\]

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पाठ 12: Aldehydes, Ketones and Carboxylic Acids - Multiple Choice Questions (Type - I) [पृष्ठ १७६]

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एनसीईआरटी एक्झांप्लर Chemistry [English] Class 12
पाठ 12 Aldehydes, Ketones and Carboxylic Acids
Multiple Choice Questions (Type - I) | Q 50 | पृष्ठ १७६

संबंधित प्रश्‍न

How will you convert ethanal into the following compound?

Butane-1, 3-diol


Write structural formulas and names of four possible aldol condensation products from propanal and butanal. In each case, indicate which aldehyde acts as nucleophile and which as electrophile.


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

\[\begin{array}{cc}
\ce{C6H5CHO}\phantom{............}\\
\phantom{........}\ce{+\phantom{......}\ce{->[dil.NaOH][\Delta]}}\phantom{...}\\
\ce{CH3CH2CHO}\phantom{............}
\end{array}\]


Compounds A and C in the following reaction are:

\[\ce{CH3CHO ->[(i) CH3MgBr][(ii) H2O] (A) ->[H2SO4, Δ] (B) ->[Hydroboration oxidation] (C)}\]


Why is there a large difference in the boiling points of butanal and butan-1-ol?


Why are carboxylic acids more acidic than alcohols or phenols although all of them have hydrogen atom attached to a oxygen atom \[\ce{(-O-H)}\]?


Assertion: Aromatic aldehydes and formaldehyde undergo Cannizaro reaction.

Reason: Aromatic aldehydes are almost as reactive as formaldehyde.


Cross aldol condensation occurs between


Identify A and B from the following reaction:

\[\begin{array}{cc}
\ce{CH3}\phantom{.................}\\
|\phantom{....................}\\
\phantom{}\ce{2CH3 - C = O ->[Ba(OH)2] A ->[Δ] B + H2O}
\end{array}\]


Convert the following:

Acetaldehyde to But-2-enal


Predict the reagent for carrying out the following transformations:

Ethanal to 3-hydroxy butanal


\[\ce{CH3-CH2-CHO ->[dil][alkali] Product}\]

The product in the above reaction is:


Explain Aldol condensation of ethanal.


Which of the following does not give aldol condensation reaction?


Why is the α-hydrogens of aldehydes and ketones are acidic in nature?


Assertion (A): The final product in Aldol condensation is always α, β-unsaturated carbonyl compound.

Reason (R): α, β-unsaturated carbonyl compounds are stabilised due to conjugation.


Identify A and B:


When acetaldehyde is treated with dilute NaOH, the following reaction is observed.

\[\begin{array}{cc}
\ce{2CH3 - CHO ->[dil.NaOH] CH3 - CH - CH2 - CHO}\\
\phantom{...............}|\\
\phantom{.................}\ce{OH}
\end{array}\]

  1. What are the functional groups in the product?
  2. Can another product be formed during the same reaction? (Deduce the answer by doing atomic audit of reactant and product).
  3. Is this an addition reaction or condensation reaction?

Write a note on the aldol condensation reaction of acetaldehyde.


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