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What are ambident nucleophiles? Explain with an example.
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Which compound in the following pair will react faster in SN2 reaction with OH−?
CH3Br or CH3I
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Which compound in the following pair will react faster in SN2 reaction with OH−?
(CH3)3CCl or CH3Cl
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How will you bring about the following conversion?
Toluene to benzyl alcohol
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Write the structure of the major organic product in the following reaction:
\[\ce{CH3CH(Br)CH2CH3 + NaOH ->[water]}\]
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Write the structure of the major organic product in the following reaction:
\[\ce{CH3CH2Br + KCN ->[aq.ethanol]}\]
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Write the structure of the major organic product in the following reaction:
\[\ce{CH3CH2CH2OH + SOCl2 ->}\]
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Write the mechanism of the following reaction:
\[\ce{{n}BuBr + KCN ->[EtOH-H2O] {n}BuCN}\]
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Arrange the compounds of the following set in order of reactivity towards SN2 displacement:
2-Bromo-2-methylbutane, 1-Bromopentane, 2-Bromopentane
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Arrange the compounds of the following set in order of reactivity towards SN2 displacement:
1-Bromo-3-methylbutane, 2-Bromo-2-methylbutane, 2-Bromo-3-methylbutane
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Arrange the compounds of the following set in order of reactivity towards SN2 displacement:
1-Bromobutane, 1-Bromo-2, 2-dimethylpropane, 1-Bromo-2-methylbutane, 1-Bromo-3-methylbutane
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Out of C6H5CH2Cl and C6H5CHClC6H5, which is more easily hydrolysed by aqueous KOH.
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The treatment of alkyl chlorides with aqueous KOH leads to the formation of alcohols but in the presence of alcoholic KOH, alkenes are major products. Explain.
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What happens when chlorobenzene is subjected to hydrolysis?
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What happens when ethyl chloride is treated with aqueous KOH?
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What happens when methyl chloride is treated with KCN?
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How the following conversion can be carried out?
Ethyl chloride to propanoic acid.
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C–Cl bond length in chlorobenzene is shorter than C–Cl bond length in CH3–Cl.
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SN1 reactions are accompanied by racemization in optically active alkyl halides.
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Orange colour of `Cr_2O_7^(2–)` ion changes to yellow when treated with an alkali. Why?
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