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Common Types of Organic Reactions(Substitution, Addition, Elimination, and Rearrangement) NEET Questions
NEET SYLLABUS
Organic Chemistry - Some Basic Principles of Organic Chemistry
Tetravalency of Carbon: Shapes of Simple Molecules
Hybridization (s and p) : Classification of Organic Compounds Based on Functional Groups
Halogens, Oxygen, Nitrogen, and Sulphur
Homologous Series - Isomerism - Structural and Stereoisomerism
Nomenclature (Trivial and IUPAC)
Covalent Bond Fission -Homolytic and Heterolytic, Free Radicals, Carbocations and Carbanions,...
Electronic Displacement in a Covalent Bond ( Inductive Effect, Electromeric Effect, ... )
Common Types of Organic Reactions(Substitution, Addition, Elimination, and Rearrangement)
Common Types of Organic Reactions(Substitution, Addition, Elimination, and Rearrangement) MCQ Questions
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7.
Which carbon centre is most likely to undergo SN1 reaction the fastest?
A.
Primary (1°) carbon
B.
Vinylic carbon
C.
Tertiary (3°) carbon
D.
Methyl carbon
😑
View Answer
Rough Work
Error
ANSWER
:
C. Tertiary (3°) carbon
8.
Which substrate is most reactive in an SN2 reaction?
A.
CH3CH2C(CH3)2Br
B.
(CH3)3CBr
C.
(CH3)2CHBr
D.
CH3Br
😑
View Answer
Rough Work
Error
ANSWER
:
D. CH3Br
9.
The SN2 mechanism is characterized by:
A.
Retention of configuration
B.
Inversion of configuration (Walden inversion)
C.
Racemisation
D.
No stereochemical change
😑
View Answer
Rough Work
Error
ANSWER
:
B. Inversion of configuration (Walden inversion)
10.
Which of the following is the BEST leaving group in nucleophilic substitution?
A.
F⁻
B.
NH2⁻
C.
OH⁻
D.
I⁻
😑
View Answer
Rough Work
Error
ANSWER
:
D. I⁻
11.
Friedel-Crafts alkylation of benzene with CH3Cl in presence of anhydrous AlCl3 produces:
A.
Toluene (methylbenzene)
B.
Cyclohexane
C.
Chlorobenzene
D.
Benzyl chloride
😑
View Answer
Rough Work
Error
ANSWER
:
12.
In the reaction CH3COCH3 + HCN → (CH3)2C(OH)(CN), the CN⁻ acts as a:
A.
Lewis acid
B.
Nucleophile (nucleophilic addition)
C.
Free radical
D.
Electrophile
😑
View Answer
Rough Work
Error
ANSWER
:
B. Nucleophile (nucleophilic addition)
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