The IUPAC name of the given compound is-



1. Hexa-1,3-dien-5-yne
2.
Hexa-3,5-dien-1-yne
3.
Hexa-1,3-en-5-yne
4. Hexane-1,3-dien-5-yne

Subtopic:  Nomenclature |
 71%
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Match the structures given in column I with the corresponding IUPAC names given in column II and choose the correct option.

Column I Column II
A. i. Pent-4-en-2-ol
B. ii.  Cyclohex-2-en-1-ol
C. iii. 6-Hydroxy-heptanal
D. iv. 2-Chlorohexane
E. v. 3- Nitrocyclohexene

1. A=iii; B= iv; C=v; D=ii; E=i
2. A=iii; B= iv; C=ii; D=v; E=i
3. A=iv; B= i; C=v; D=iii; E=ii
4. A=iv; B= i; C=ii; D=v; E=iii

Subtopic:  Nomenclature |
 92%
From NCERT
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Match the items in column I with the items in column II.

Column I Column II
a. o-Ethylanisole i.
b.  p-Nitroaniline ii.
c. 2,3 - Dibromo -1 - phenylpentane iii.
d. 4-Ethyl-1-fluoro-2-nitrobenzene iv.


The correct option is-
1. a=ii; b=iv; c=i; d=iii
2. a=ii; b=i; c=iv; d=iii
3. a=iv; b=i; c=ii; d=iii
4. a=ii; b=iii; c=iv; d=i

Subtopic:  Nomenclature |
 92%
From NCERT
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The incorrect curved-arrow notation that shows the formation of reactive intermediates in the following compound is-

1.
2.
3.
4. All of the above
Subtopic:  Bond Cleavage & Isomerism |
 59%
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Match column I with Column-II.
 
Column I
(Molecules)
COLUMN II
(Nature of molecule) 
a. (CH3)3N: i. Electrophile
b. \(H_3C-\overset{+}{C}=O\) ii. Nucleophile
c. \(\overset{+}{N}O_2\)
d. H2N:-
 
a b c d
1. ii ii ii i
2. ii ii ii ii
3. ii i i ii
4. ii i ii ii
Subtopic:  Nucleophile & Electrophile |
 84%
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Consider the following molecule.

(a) H3C-H, H3C-Br

(b) H3C-NH2, H3C-OH

(c) H3C-OH, H3C-SH

The bond which is more polar in the given pairs of molecules is-

1. C-H bond is more polar than C-Br bond; C-O is more polar than C-N and C-S bond
2. C-Br bond is more polar than C-H bond; C-O is more polar than C-N and C-S bond
3. C-Br bond is more polar than C-H bond; C-N is more polar than C-O and C-O bond is more polar than C-S
4. None of the above


 

Subtopic:  Aromaticity & Polarity |
 73%
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Consider the following compound:
 
Carbon with minimum impact of negative inductive effect of Br is -

1. C1
2. C2
3. C3
4. All have same inductive effect


 

Subtopic:  Electron Displacement Effects |
 89%
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The correct resonance structures of CH3COO- among the following are-
 

1.
2.
3.
4.





 

Subtopic:  Electron Displacement Effects |
 83%
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Consider the possible resonating structures of CH2=CH–CHO is as follows:


The correct sequence of stability is-

1. II > I > III
2. III > I > II
3. I > III > II
4. I > II > III

Subtopic:  Electron Displacement Effects |
 78%
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Consider the resonance structure of CH3COOCHas follows:



The correct statement among the following is-

1. I and II cannot be the major contributors to the real structure of CH3COOCH3
2. I and II can be the major contributors to the real structure of CH3COOCH3
3. I is more stable than II.
4. None of the above





 

Subtopic:  Electron Displacement Effects |
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