Q 1 :    

Number of alkanes obtained on electrolysis of a mixture of CH3COONa and C2H5COONa is _________ .                  [2024]



(3)

     Kolbe's electrolysis of RCOO-Na+ gives R-R

     2RCOONa+2H2OelectrolysisR-R+2CO2+2NaOH+H2

     Thus electrolysis of mixture of CH3COONa and C2H5COONa gives three alkanes: CH3-CH3, C2H5-C2H5 and CH3-C2H5

 



Q 2 :    

The incorrect statement regarding conformations of ethane is:                          [2024]

  • Ethane has infinite number of conformations.

     

  • The dihedral angle in staggered conformation is 60°.

     

  • Eclipsed conformation is the most stable conformation.

     

  • The conformations of ethane are inter-convertible to one-another.

     

(3)

 



Q 3 :    

3-Methylhex-2-ene on reaction with HBr in presence of peroxide forms an addition product (A). The number of possible stereoisomers for ‘A’ is ______.           [2024]



(4)

Major product (A) has two chiral centres and from mechanism of this reaction it is clear that both R and S configurations are possible at both these chiral centres. Hence A has 22=4 stereoisomers.



Q 4 :    

When sec-butylcyclohexane reacts with bromine in the presence of sunlight, the major product is :                [2025]

  • [IMAGE 109]

     

  • [IMAGE 110]

     

  • [IMAGE 111]

     

  • [IMAGE 112]

     

(4)

In free radical bromination of alkanes, that product is major which is formed by most stable free radical intermediate. Stability of free radicals is 3° > 2° > 1°. Out of two 3° carbons present in sec-butylcyclohexane, carbon I forms more stable free radical as it has more number of α H atoms.

[IMAGE 113]

 

 



Q 5 :    

[IMAGE 114]

The maximum number of RBr producing 2-methylbutane by above sequence of reactions is ______. (Consider the structural isomers only)       [2025]

  • 4

     

  • 1

     

  • 3

     

  • 5

     

(1)

RBrMg+EtherR-Mg-BrH2ORH+Mg(OH)Br

Possible structural isomers of R–Br for RH = 2-methylbutane are obtained by placing Br at any one of the following four places:

[IMAGE 115]

 



Q 6 :    

Propane molecule on chlorination under photochemical condition gives two di-chloro products, “x” and “y”. Amongst “x” and “y”, “x” is an optically active molecule. How many tri-chloro products (consider only structural isomers) will be obtained from “x” when it is further treated with chlorine under the photochemical condition.        [2025]

  • 3

     

  • 2

     

  • 5

     

  • 4

     

(1)

[IMAGE 116]