Home
Class 12
CHEMISTRY
SN^2 is favoured by...

`SN^2` is favoured by

A

Polar solvent

B

non polar sovent

C

More branching

D

Weak nucleophile

Text Solution

Verified by Experts

The correct Answer is:
B
`SN^2` reaction
Doubtnut Promotions Banner Mobile Dark
|

Topper's Solved these Questions

  • HALOGEN DERIVATIVES OF ALKANES (AND ARENES)

    MARVEL PUBLICATION|Exercise TEST YOUR GRASP|15 Videos

  • HALOGEN DERIVATIVES OF ALKANES (AND ARENES)

    MARVEL PUBLICATION|Exercise HIGHER LEVEL|69 Videos

  • GENERAL PRINCIPLES AND PROCESSES OF ISOLATION OF ELEMENTS

    MARVEL PUBLICATION|Exercise Test Your Grasp|30 Videos

  • ORGANIC COMPOUNDS CONTAINGING NITROGEN

    MARVEL PUBLICATION|Exercise TEST YOUR GRASP|40 Videos

Similar Questions

Explore conceptually related problems

SN2 Mechanism

In which alkyl halide SN^(2) mechanism is favoured maximum

Knowledge Check

  • S_N^1 reaction is favoured by

    A
    Non - polar solvents
    B
    Bulky alkyl groups on the carbon atom attached to halogen atom
    C
    Less steric hindrance containing akyl halides
    D
    Less stable carbocation

  • Which one of the following was favoured by Nehru but not favoured by Gandhi?

    A
    Truth
    B
    Non-violence
    C
    Untouchability
    D
    Heavy-idustrialization

  • Which one of the following was favoured by Nehru but not favoured by Gandhiji?

    A
    Truth
    B
    Non-violence
    C
    Untouchability
    D
    Heavy industrialization

    • Similar Questions

    Explore conceptually related problems

    The first steps of SN^(1) and SN^(2) recatiosns are, respectively

    Nucleophilic substitution reactions are of two types, substitution nucleophllic bimolecular (SN^2) and substitution nucleophilic unimolecular (SN^1) depending on molecules taking part in determining the rate of reaction. Reactivity of alkyl halide towards SN^1 and SN^2 reactions depends on various factors such as steric hindrance, stability of intermediate or transition state and polarity of solvent. SN^2 reaction mechanism is favoured mostly by primary alkyl halide then secondary and then tertiary. This order is reversed in case of SN^1 reactions. In the following pairs of halogen compounds, which would undergo SN^2 reaction faster.

    Nucleophilic substitution reactions are of two types, substitution nucleophllic bimolecular (SN^2) and substitution nucleophilic unimolecular (SN^1) depending on molecules taking part in determining the rate of reaction. Reactivity of alkyl halide towards SN^1 and SN^2 reactions depends on various factors such as steric hindrance, stability of intermediate or transition state and polarity of solvent. SN^2 reaction mechanism is favoured mostly by primary alkyl halide then secondary and then tertiary. This order is reversed in case of SN^1 reactions. In the following pairs of halogen compounds, which would undergo SN^2 reaction faster.

    Nucleophilic substitution reactions are of two types, substitution nucleophllic bimolecular (SN^2) and substitution nucleophilic unimolecular (SN^1) depending on molecules taking part in determining the rate of reaction. Reactivity of alkyl halide towards SN^1 and SN^2 reactions depends on various factors such as steric hindrance, stability of intermediate or transition state and polarity of solvent. SN^2 reaction mechanism is favoured mostly by primary alkyl halide then secondary and then tertiary. This order is reversed in case of SN^1 reactions. In the following pairs of halogen compounds, which would undergo SN^2 reaction faster.

    Nucleophilic substitution reactions are of two types, substitution nucleophllic bimolecular (SN^2) and substitution nucleophilic unimolecular (SN^1) depending on molecules taking part in determining the rate of reaction. Reactivity of alkyl halide towards SN^1 and SN^2 reactions depends on various factors such as steric hindrance, stability of intermediate or transition state and polarity of solvent. SN^2 reaction mechanism is favoured mostly by primary alkyl halide then secondary and then tertiary. This order is reversed in case of SN^1 reactions. In the following pairs of halogen compounds, which would undergo SN^2 reaction faster.

    Home
    Profile