Chemistry-
General
Easy
Question
and are-
- Chain isomers
- Position isomers
- Functional isomers
- None of these
The correct answer is: Functional isomers
Related Questions to study
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The IUPAC name of the given compound is -
The IUPAC name of the given compound is -
chemistry-General
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and are-
and are-
chemistry-General
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and & are called as -
and & are called as -
chemistry-General
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Identify the end product (B) of the following sequence of reaction.
Identify the end product (B) of the following sequence of reaction.
chemistry-General
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Following two isomers are -
Following two isomers are -
chemistry-General
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Number of optically active isomers of tartaric acid is -
Number of optically active isomers of tartaric acid is -
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The number of optically active isomers possible in -
The number of optically active isomers possible in -
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The absolute configuration of the compound is -
The absolute configuration of the compound is -
chemistry-General
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If optical rotation produced by the compound [A] is +65°, then produced by the compound
If optical rotation produced by the compound [A] is +65°, then produced by the compound
chemistry-General
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The correct statement about the compound (A), (B) and (C) is -
A)
B)
C)
The correct statement about the compound (A), (B) and (C) is -
A)
B)
C)
chemistry-General
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Urea molecule exhibit -
Urea molecule exhibit -
chemistry-General
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Which is a pair of geometrical isomers -
I)
II)
III)
IV)
Which is a pair of geometrical isomers -
I)
II)
III)
IV)
chemistry-General
chemistry-
Choose the group showing position isomerism -
a)
b)
c)
d)
e)
Choose the group showing position isomerism -
a)
b)
c)
d)
e)
chemistry-General
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Type of isomerism exists between and
Type of isomerism exists between and
chemistry-General
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Assertion : tert-Butoxide is a stronger base than or ion but is a much poor nucleophile.
Reason : A negatively charged ions is always more powerful nucleophile than its conjugate acid.
Assertion : tert-Butoxide is a stronger base than or ion but is a much poor nucleophile.
Reason : A negatively charged ions is always more powerful nucleophile than its conjugate acid.
chemistry-General