In the given conversion the compound A is:
In the given conversion the compound A is:
The Correct Option is B
Solution and Explanation
The correct option is: (B)
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Questions Asked in JEE Main exam
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Statement (I): NaCl is added to the ice at \( 0^\circ C \), present in the ice cream box to prevent the melting of ice cream.
Statement (II): On addition of NaCl to ice at \( 0^\circ C \), there is a depression in freezing point.
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- Let circle $C$ be the image of
$$ x^2 + y^2 - 2x + 4y - 4 = 0 $$
in the line
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and $A$ be the point on $C$ such that $OA$ is parallel to the x-axis and $A$ lies on the right-hand side of the centre $O$ of $C$.
If $B(\alpha, \beta)$, with $\beta < 4$, lies on $C$ such that the length of the arc $AB$ is $\frac{1}{6}$ of the perimeter of $C$, then $\beta - \sqrt{3}\alpha$ is equal to: - A force \( \mathbf{F} = 2\hat{i} + b\hat{j} + \hat{k} \) is applied on a particle and it undergoes a displacement \( \mathbf{r} = \hat{i} - 2\hat{j} - \hat{k} \). What will be the value of \( b \), if the work done on the particle is zero?
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Let one focus of the hyperbola \( H : \dfrac{x^2}{a^2} - \dfrac{y^2}{b^2} = 1 \) be at \( (\sqrt{10}, 0) \) and the corresponding directrix be \( x = \dfrac{9}{\sqrt{10}} \). If \( e \) and \( l \) respectively are the eccentricity and the length of the latus rectum of \( H \), then \( 9 \left(e^2 + l \right) \) is equal to:
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Concepts Used:
Organic Chemistry – Some Basic Principles and Techniques - Reaction Mechanism
SN1 Reaction Mechanism:
SN1 reaction mechanism takes place by following three steps –
- Formation of carbocation
- Attack of nucleophile
- Deprotonation
SN2 Reaction Mechanism:
The SN2 reaction mechanism involves the nucleophilic substitution reaction of the leaving group (which generally consists of halide groups or other electron-withdrawing groups) with a nucleophile in a given organic compound.
Electrophilic Aromatic Substitution Reaction Mechanism:
The mechanism of an electrophilic aromatic substitution reaction contains three main components which are:
- A new sigma bond from C=C is formed during the reaction in the arene nucleophile.
- Due to the breaking of the C-H sigma bond, a proton is removed.
- The C=C bond is reformed and it restores the aromaticity of the compound.
Electrophilic Substitution Reaction Mechanism:
The electrophilic substitution reaction mechanism is composed of three steps, which will be discussed more below.
- Electrophile Generation
- Carbocation Formation
- Proton Removal