मराठी

An organic compound 'A' with the molecular formula C4H8O2 undergoes acid hydrolysis to form two compounds 'B' and 'C'. - Chemistry

Advertisements
Advertisements

प्रश्न

An organic compound 'A' with the molecular formula C4H8O2 undergoes acid hydrolysis to form two compounds 'B' and 'C'. Oxidation of 'C' with acidified potassium permanganate also produces 'B'. Sodium salt of 'B' on heating with soda lime gives methane.

  1. Identify 'A', 'B' and 'C'.
  2. Out of 'B' and 'C', which will have higher boiling point? Give reason.
थोडक्यात उत्तर
Advertisements

उत्तर

  1. A = C4H8O2 [CH3COOC2H5] ester Reactions involved are
    \[\ce{\underset{A}{CH3-COOC2H5} + H2O ->[dil H2SO4] \underset{B}{CH3COOH} + \underset{C}{CH3CH2OH}}\]
    Then
    \[\ce{\underset{C}{CH3CH2OH} ->[KMnO4][{[O]}] \underset{B}{CH3COOH}}\]
    So A = CH3COOC2H5, B = CH3COOH, C = CH3CH2OH
  2. B has a higher boiling point than C. Because of their propensity to generate intermolecular H-bonds, carboxylic acids have higher boiling temperatures than alcohols.
shaalaa.com
  या प्रश्नात किंवा उत्तरात काही त्रुटी आहे का?
2022-2023 (March) Delhi Set 1

व्हिडिओ ट्यूटोरियलVIEW ALL [1]

संबंधित प्रश्‍न

Give a simple chemical test to distinguish between the following pair of compounds:

Ethanal and Propanal


Out of CH3CH2 – CO – CH2 – CH3 and CH3CH2 – CH2 – CO – CH3, which gives iodoform test?


How will you convert ethanal into the following compound?

But-2-enoic acid


An organic compound contains 69.77% carbon, 11.63% hydrogen and rest oxygen. The molecular mass of the compound is 86. It does not reduce Tollens’ reagent but forms an addition compound with sodium hydrogensulphite and give positive iodoform test. On vigorous oxidation it gives ethanoic and propanoic acid. Write the possible structure of the compound.


\[C_6 H_5 - OH \to^{{Br}_2 \left( aq \right)} ?\]

Alkenes decolourise bromine water in presence of CCl4 due to formation of ______.


A hydrocarbon (A) with molecular formula C5H10 on ozonolysis gives two products (B) and (C). Both (B) and (C) give a yellow precipitate when heated with iodine in presence of NaOH while only (B) give a silver mirror on reaction with Tollen’s reagent.

  1. Identify (A), (B) and (C).
  2. Write the reaction of B with Tollen’s reagent.
  3. Write the equation for iodoform test for C.
  4. Write down the equation for aldol condensation reaction of B and C.

Which among the above compound/s does/do not form Silver mirror when treated with Tollen's reagent?


The correct set of products obtained in the following reactions:

  1. \[\ce{RCN ->[reduction]}\]
  2. \[\ce{RCN ->[(i) CH3MgBr][(ii) H2O]}\]
  3. \[\ce{RNC ->[hydrolysis]}\]
  4. \[\ce{RNH2 ->[HNO2]}\]

In Tollen's test for aldehyde, the overall number of electrons(s) transferred to the Tollen's reagent formula \[\ce{[Ag(NH3)2]+}\] per aldehyde group to form silver mirror is ______. (Round off to the nearest integer)


Share
Notifications

Englishहिंदीमराठी


      Forgot password?
Use app×