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Concept explainers
(a)
Interpretation:
To classify each carbocation as 1°, 2°, or 3°.
Concept introduction:
SN2 reaction is a special type of reaction mechanism in
(b)
Interpretation:
To classify each carbocation as 1°, 2°, or 3°.
Concept introduction:
SN2 reaction is a special type of reaction mechanism in organic chemistry. It is kind of nucleophilic substitution reaction. Nucleophilic substitutions are Lewis acid-base reactions. In this reaction the nucleophile donates its electron pair, the alkyl halide (Lewis acid) accepts it, and the C-X bond is heterolytically cleaved. Alkyl halides are organic molecules that contains a halogen atom X bonded to sp3 hybridized carbon atom. Alkyl halides are classified as primary (1°), secondary (2°), and tertiary (3°) depending on the number of carbons bonded to the carbon with the halogen. In this reaction carbocation cannot form because it is an intermediate formed in the SN1 reaction.
(c)
Interpretation:
To classify each carbocation as 1°, 2°, or 3°.
Concept introduction:
SN2 reaction is a special type of reaction mechanism in organic chemistry. It is kind of nucleophilic substitution reaction. Nucleophilic substitutions are Lewis acid-base reactions. In this reaction the nucleophile donates its electron pair, the alkyl halide (Lewis acid) accepts it, and the C-X bond is heterolytically cleaved. Alkyl halides are organic molecules that contains a halogen atom X bonded to sp3 hybridized carbon atom. Alkyl halides are classified as primary (1°), secondary (2°), and tertiary (3°) depending on the number of carbons bonded to the carbon with the halogen. In this reaction carbocation cannot form because it is an intermediate formed in the SN1 reaction.
(d)
Interpretation:
To classify each carbocation as 1°, 2°, or 3°.
Concept introduction:
SN2 reaction is a special type of reaction mechanism in organic chemistry. It is kind of nucleophilic substitution reaction. Nucleophilic substitutions are Lewis acid-base reactions. In this reaction the nucleophile donates its electron pair, the alkyl halide (Lewis acid) accepts it, and the C-X bond is heterolytically cleaved. Alkyl halides are organic molecules that contains a halogen atom X bonded to sp3 hybridized carbon atom. Alkyl halides are classified as primary (1°), secondary (2°), and tertiary (3°) depending on the number of carbons bonded to the carbon with the halogen. In this reaction carbocation cannot form because it is an intermediate formed in the SN1 reaction.
(e)
Interpretation:
To classify each carbocation as 1°, 2°, or 3°.
Concept introduction:
SN2 reaction is a special type of reaction mechanism in organic chemistry. It is kind of nucleophilic substitution reaction. Nucleophilic substitutions are Lewis acid-base reactions. In this reaction the nucleophile donates its electron pair, the alkyl halide (Lewis acid) accepts it, and the C-X bond is heterolytically cleaved. Alkyl halides are organic molecules that contains a halogen atom X bonded to sp3 hybridized carbon atom. Alkyl halides are classified as primary (1°), secondary (2°), and tertiary (3°) depending on the number of carbons bonded to the carbon with the halogen. In this reaction carbocation cannot form because it is an intermediate formed in the SN1 reaction.
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Chapter 7 Solutions
Organic Chemistry-Package(Custom)
- 1) identify the reactant/s in the chemical equation and circle it, also name its major functional group 2) identify the product/s in the chemical equation (circle it) and name its functional group 3) is the a reversible reaction or not? How do we knowarrow_forwardLabel each pair of alkenes as constitutional isomers, stereoisomers, or identical. А. and constitutional B. and isomers identical stereoisomers C. CH3 and H. constitutional isomers CH3 CH3 CH3CH2 CH2CH3 CH3CH2 CH3 D. and CH3 CH3 CH3 CH2CH3 I-arrow_forwardClassify each alkyl halide as 1 °, 2 °, or 3 °.arrow_forward
- Which statement is true? O Bromination is faster than chlorination because the rate-determining step for bromination is endothermic. O Bromination is slower than chlorination because the rate-determining step for bromination is endothermic. O Bromination is faster than chlorination because the rate-determining step for bromination is exothermic. O Bromination is slower than chlorination because the rate-determining step for bromination is exothermic.arrow_forwardDraw the products formed (including stereoisomers) in each reaction.arrow_forwardClassify the carbocations as 1°, 2°, or 3°, and rank the carbocations in each group in order of increasing stability.arrow_forward
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