Multiple Choice QuestionsGiven are cyclohexanol (I), acetic acid (II), 2,4,6-trinitropenol (III) and phenol (IV). In these, the order of decreasing acidic character will be
III > II> IV> I
II > III> I > IV
II > III> IV> I
II > III> IV> I
Which one is most reactive towards electrophilic reagent?
A.
Electron withdrawing substituent deactivates the benzene nucleus towards electrophilic substitution while electron releasing substituent activates the ring towards electrophilic substitution.
Among the given -OH has the higher electron donating tendency and thus, activates the ring more towards electrophilic substitution. Hence
is more reactive towards electrophilic reagents.
Among the following four compounds
A) Phenol
B) Methyl Phenol
C) meta - nitrophenol
D) para-nitrophenol
the acidity order is
D > C > A > B
C > D > A> B
A > D > C > B
A > D > C > B
Consider the following reaction,
the product,Z,is
toluene
benzaldehyde
benzoic acid
benzoic acid
The order of decreasing reactivity towards an electrophilic reagent, for the following:
i) Benzene
ii) Toluene
iii) Chlorobenzene
iv) Phenol
would be:
(i) > (ii) > (iii) > (iv)
(ii) > (iv) > (i) > (iii)
(iv) > (iii) > (ii) >(i)
(iv) > (iii) > (ii) >(i)
The major organic product in the reaction,
CH3 -O- CH(CH3)2 + HI → Product is:
CH3OH + (CH3)2 + CHI
ICH2OCH(CH3)2
CH3O CI(CH3)2
CH3O CI(CH3)2
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