Home
Class 12
CHEMISTRY
An organic compoud [A] which has charact...

An organic compoud [A] which has characteristic odour on treatment with `NaOH` forms two compounds [B] and [C]. Compounds [B] has the molecule formula `C_(7)H_(8)O`. Which on oxidation gives back compound [A]-The compound [C] is the sodium salt of an acid [C]. When [C] is heated with sodalime, it yield an aromatic hydrocarbon [D]. Deduce the structures of [A], [B], [C] and [D].

Text Solution

AI Generated Solution

To deduce the structures of compounds [A], [B], [C], and [D], let's analyze the information provided step by step. ### Step 1: Identify Compound [A] The question states that compound [A] has a characteristic odor and reacts with NaOH to form two products. Given that it is an organic compound with a characteristic odor, it is likely an aromatic aldehyde. **Conclusion**: - Compound [A] is **Benzaldehyde (C₇H₆O)**, which has the structure: ...
Promotional Banner

Topper's Solved these Questions

  • ALDEHYDES AND KETONES

    DINESH PUBLICATION|Exercise Additional Important Question|35 Videos
  • ALDEHYDES AND KETONES

    DINESH PUBLICATION|Exercise Question From Board|86 Videos
  • ALDEHYDES AND KETONES

    DINESH PUBLICATION|Exercise Interger|5 Videos
  • ALCOHOLS AND PHENOLS

    DINESH PUBLICATION|Exercise Matrix|9 Videos
  • ALKALI EARTH METALS

    DINESH PUBLICATION|Exercise Unit test-12|5 Videos

Similar Questions

Explore conceptually related problems

(a) An organic compound (A) has characteristic odour . On treatment with NaOH it forms two compounds (B) and (C ) compound (B ) has molecular formula C_7 H_8 O which on oxidation gives back (A ) . The compound (C ) is a sodium salt of an acid. When (C) is treated with soda lime it yields an aromatic hydrocarbon (D).Deduce the structures of (A ) ,(B ) , (C ) and (D ) write the sequence of reactions involved . (b) complete each synthesis by filling the missing starting materials reagents or products (x,y and z ) (i) C_6 H_5 CHO +CH_3 CH_2 CHO overset(NaOH ) to X (ii) CH_3 (CH_2) _9 COOC _2 H_5 overset(Z)to CH_3 (CH_2) _9 CHO (c) How will you bring about the following conversions in not more than two steps (i) Toluene to benzaldehyde (ii) Ethylcyanide to 1- Phenylpropanone .

A compound [A] of molecular formula C_(4)H_(9)Br yields a compound [B] of molecular formula C_(4)H_(10)O when reated with aqueous NaOH . On oxidation [B] gives a ketone [C]. The vigorous oxidation of ketone gives ethanoic acid. Dutuce the structure of A, B and C.

An organic compound [A] with molecular formula C_(4)H_(8)O when reduced with NaBH_(4) gives compound [B] which reacts with HBr to form compound [C] (optically active) Identify A,B , C and wirte the two enantimoers of compound [C].