Home
Class 12
CHEMISTRY
Phenyl subsituted hydrocarbon (A) molecu...

Phenyl subsituted hydrocarbon (A) molecular mass 120 on monobromination can give 3 isomeric products only Major product (B) on treatment with sodium gives (C). Find (A) (B) and (C)

Text Solution

AI Generated Solution

To solve the problem, we need to identify the phenyl substituted hydrocarbon (A), the major product from its monobromination (B), and the product formed when (B) is treated with sodium (C). ### Step-by-Step Solution: **Step 1: Determine the structure of hydrocarbon (A)** - Given that (A) is a phenyl substituted hydrocarbon with a molecular mass of 120 g/mol. - The molecular formula of the phenyl group (C6H5) has a mass of 77 g/mol (6 carbons and 5 hydrogens). - Therefore, the remaining mass for the substituent is 120 - 77 = 43 g/mol. ...
Promotional Banner

Topper's Solved these Questions

  • HYDROCARBONS

    AAKASH INSTITUTE ENGLISH|Exercise SECTION-J AAKASH CHALLENGERS QUESTIONS|5 Videos
  • HYDROCARBONS

    AAKASH INSTITUTE ENGLISH|Exercise Try yourself|78 Videos
  • HYDROCARBONS

    AAKASH INSTITUTE ENGLISH|Exercise SECTION-H MULTIPLE TRUE-FALSE TYPE QUESTIONS|2 Videos
  • HALOALKANES AND HALOARENES

    AAKASH INSTITUTE ENGLISH|Exercise ASSIGNMENT SECTION -D|15 Videos
  • HYDROGEN

    AAKASH INSTITUTE ENGLISH|Exercise ASSIGNMENT (SECTION - D) (Assertion-Reason Type question)|15 Videos

Similar Questions

Explore conceptually related problems

A hydrocarbon of molecular formula C_(6)H_(14) on monochlorination given two products Identify the structure of hydrocarbon.

Predict the major products (A) , (B) & (C )

Find the product C(major) .

Identify number of reactions that can give benzene as major product

Which of the following alkane upon dichlorination can give only two products ?

A hydrocarbon of melecular formula C_(5)H_(10) on monochlorination gives one product and on dichlorination gives three products (excluding stereoisomers) . Identify the hydrocarbon .

An alkali metal A gives a compound B (molecular mass = 40) on reacting with water. The compound B gives a soluble compound C on treatment with aluminium oxide. Identify A, B and C and give the reactions involved.

a. Give the structure of lowest molecular mass and optically active alkyne. b. Give the structure of unsaturated hydrocarbon with lowest molecular mass showing diastereomers. c. Give the structure of alkyne that gives the same product on reaction with either H_2+Ni_2B or K+C_2H_5OH . d. Give the structure of alkyne that gives the same single product on reaction with either (B_2H_6//THF+H_2O_2//overset(Ө)H) or dil. H_2SO_4//Hg^(2+)//H^(o+) . e. Give the structure of alkyne that gives the same two products with either of the reagents in (d).

Give the products (B) and (C) in the above reaction.