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प्रश्न
Compound ‘A’ with molecular formula \[\ce{C4H9Br}\] is treated with aq. \[\ce{KOH}\] solution. The rate of this reaction depends upon the concentration of the compound ‘A’ only. When another optically active isomer ‘B’ of this compound was treated with aq. \[\ce{KOH}\] solution, the rate of reaction was found to be dependent on concentration of compound and \[\ce{KOH}\] both.
(i) Write down the structural formula of both compounds ‘A’ and ‘B’.
(ii) Out of these two compounds, which one will be converted to the product with inverted configuration.
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उत्तर
(i) The molecular formulae of isomers of \[\ce{C4H9Br}\] are \[\ce{CH3}\]
\[\begin{array}{cc}
\ce{CH3}\phantom{......}\\
|\phantom{.........}\\
\ce{CH3 - C - Br}\phantom{...........}\\
|\phantom{.........}\\
\ce{\underset{2 - Bromo-2-methyl propane (A)}{CH3}}\phantom{......}
\end{array}\]
\[\begin{array}{cc}
\ce{CH3 - CH2 - CH - CH3}\\
\phantom{.....}|\phantom{}\\
\phantom{.......}\ce{\underset{2-Bromobutance (B)}{Br}}\phantom{}
\end{array}\]
Since the rate of reaction of compound ‘A’ \[\ce{(C4H9Br)}\] with aqueous \[\ce{KOH}\] depends upon the concentration of compound ‘A’ only, therefore, the reaction occurs by SN1 mechanism and compound ‘A’ is tertiary bromide i.e., 2-Bromo-2-methylpropane.
\[\ce{(CH3)3CBr + KOH(aq) –> (CH3)3COH + KBr}\]
Rate = \[\ce{A:[(CH3)3CBr]}\]
(ii) Since compound ‘B’ is optically active and is an isomer of compound ‘A’ \[\ce{(C4H9Br)}\], therefore, compound ‘B’ must be 2-Bromobutane. Since the rate of reaction of compound ‘B’ with aqueous \[\ce{KOH}\] depends upon the concentration of compound ‘B’ and \[\ce{KOH}\], therefore, the reaction occurs by SN2 mechanism and product of hydrolysis will have inverted configuration.
\[\begin{array}{cc}
\ce{CH3CH2CHCH3 + KOH -> CH3CH2CHCH3 + KBr}\\
\phantom{..}|\phantom{...............................}|\phantom{...}\\
\phantom{..}\ce{Br}\phantom{.............................}\ce{OH}\phantom{.}
\end{array}\]
Rate = 
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संबंधित प्रश्न
Which compound in the following pair will react faster in SN2 reaction with OH−?
CH3Br or CH3I
How will you bring about the following conversion?
Toluene to benzyl alcohol
Write the structure of the major organic product in the following reaction:
\[\ce{CH3CH2Br + KCN ->[aq{.} ethanol]}\]
The stability order for carbocation is _______.
(A) 2° > 3° > 1°
(B) 3° > 2° > 1°
(C) 3° > 1° > 2°
(D) 1° > 3° > 2°
Given reasons: SN1 reactions are accompanied by racemization in optically active alkyl halides.
Halogenation of alkanes is ____________.
Which one of the following halogen compounds is difficult to be hydrolysed by SN1 mechanism?
Tertiary alkyl halides are practically inert to substitution by SN2 mechanism because of ____________.
Which of the following is the correct order of decreasing SN2 reactivity?
An important chemical method to resolve a racemic mixture makes use of the formation of ______.
Which of the following is a chiral compound?
Which of the following statements are correct about this reaction?

(i) The given reaction follows SN2 mechanism.
(ii) (b) and (d) have opposite configuration.
(iii) (b) and (d) have same configuration.
(iv) The given reaction follows SN1 mechanism.
Which of the following statements are correct about the kinetics of this reaction?

(i) The rate of reaction depends on the concentration of only (b).
(ii) The rate of reaction depends on concentration of both (a) and (b).
(iii) Molecularity of reaction is one.
(iv) Molecularity of reaction is two.
Why are aryl halides less reactive towards nucleophilic substitution reactions than alkyl halides?
Chlorination of alkanes is an example of
Assertion (A) : Nucleophilic substitution of iodoethane is easier than chloroethane.
Reason (R) : Bond enthalpy of C-I bond is less than that of C-Cl bond.
Inversion of configuration occurs in ______.
The following questions are case-based questions. Read the passage carefully and answer the questions that follow:
|
Nucleophilic Substitution: Influences of solvent polarity: The reaction rate (SN2) of 2-bromopropane and NaOH in ethanol containing 40% water is twice slower than in absolute ethanol. Hence the level of solvent polarity has an influence on both SN1 and SN2 reactions but with different results. Generally speaking, a weak polar solvent is favourable for SN2 reaction, while a strong polar solvent is favourable for SN1. Generally speaking, the substitution reaction of tertiary haloalkane is based on SN1 mechanism in solvents with a strong polarity (for example ethanol containing water). |
Answer the following questions:
(a) Why racemisation occurs in SN1? (1)
(b) Why is ethanol less polar than water? (1)
(c) Which one of, the following in each pair is more reactive towards SN2 reaction? (2)
(i) CH3 – CH2 – I or CH3CH2 – Cl
(ii)

OR
(c) Arrange the following in the increasing order of their reactivity towards SN1 reactions: (2)
(i) 2-Bromo-2-methylbutane, 1-Bromo-pentane, 2-Bromo-pentane
(ii) 1-Bromo-3-methylbutane, 2-Bromo-2-methylbutane, 2-Bromo-3- methylbutane
Which alkyl halide from the following pair would you expect to react more rapidly by an SN2 mechanism? Explain your answer.
\[\begin{array}{cc}\ce{CH3CH2CHCH3}\\
\phantom{.....}|\\
\phantom{......}\ce{Br}\\
\end{array}\] or \[\begin{array}{cc}\phantom{.......}\ce{CH3}\\
\phantom{...}|\\
\ce{H3C - C - Br}\\
\phantom{...}|\\
\phantom{.......}\ce{CH3}\\
\end{array}\]
