Easy
Represent the three types of electron movement in organic reactions.
(N/A) $i$. The electron pair from a $\pi$-bond shifts to an adjacent bond position.
$ii$. The electron pair from a $\pi$-bond shifts onto an adjacent atom.
$iii$. The electron pair from an atom shifts to an adjacent bond position.
$ii$. The electron pair from a $\pi$-bond shifts onto an adjacent atom.
$iii$. The electron pair from an atom shifts to an adjacent bond position.
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The decreasing order of acidic strengths of the following compounds is:
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View SolutionThe correct stability order of the following species is:
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View SolutionGiven below are two statements,one is labelled as Assertion $A$ and the other is labelled as Reason $R$.
Assertion $A$ : Order of acidic nature of the following compounds is $A > B > C$.
(Image shows: $A$ is $2$-chlorocyclohexanol,$B$ is $4$-fluorocyclohexanol,$C$ is $3$-methylcyclohexanol)
Reason $R$ : Fluoro is a stronger electron withdrawing group than Chloro group.
In the light of the above statements,choose the correct answer from the options given below:
Assertion $A$ : Order of acidic nature of the following compounds is $A > B > C$.
(Image shows: $A$ is $2$-chlorocyclohexanol,$B$ is $4$-fluorocyclohexanol,$C$ is $3$-methylcyclohexanol)
Reason $R$ : Fluoro is a stronger electron withdrawing group than Chloro group.
In the light of the above statements,choose the correct answer from the options given below:
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View SolutionArrange the following carbanions in decreasing order of stability $:$
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View SolutionShow the polarisation of the carbon-magnesium bond in the following structure: $CH_3-CH_2-CH_2-CH_2-MgX$.
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