(a) Interpretation: The likely mechanism of nucleophilic substitution for the given alkyl halide is to be predicted. Concept introduction: Nucleophilic substitution reaction takes place by two mechanisms, S N 1 and S N 2 . In S N 1 mechanism, formation of carbocation takes place by removal of halide and then nucleophile attack occurs on that carbocation. However in S N 2 mechanism, removal of halide and attack of nucleophile takes place simultaneously.
(a) Interpretation: The likely mechanism of nucleophilic substitution for the given alkyl halide is to be predicted. Concept introduction: Nucleophilic substitution reaction takes place by two mechanisms, S N 1 and S N 2 . In S N 1 mechanism, formation of carbocation takes place by removal of halide and then nucleophile attack occurs on that carbocation. However in S N 2 mechanism, removal of halide and attack of nucleophile takes place simultaneously.
Solution Summary: The author explains that the likely mechanism of nucleophilic substitution for the given alkyl halide is to be predicted.
Definition Definition Organic compounds in which one or more hydrogen atom in an alkane is replaced by a halogen atom (fluorine, chlorine, bromine, or iodine). These are also known as haloalkanes.
Chapter 7, Problem 7.29P
Interpretation Introduction
(a)
Interpretation: The likely mechanism of nucleophilic substitution for the given alkyl halide is to be predicted.
Concept introduction: Nucleophilic substitution reaction takes place by two mechanisms, SN1 and SN2. In SN1 mechanism, formation of carbocation takes place by removal of halide and then nucleophile attack occurs on that carbocation. However in SN2 mechanism, removal of halide and attack of nucleophile takes place simultaneously.
Interpretation Introduction
(b)
Interpretation: The likely mechanism of nucleophilic substitution for the given alkyl halide is to be predicted.
Concept introduction: Nucleophilic substitution reaction takes place by two mechanisms, SN1 and SN2. In SN1 mechanism, formation of carbocation takes place by removal of halide and then nucleophile attack occurs on that carbocation. However in SN2 mechanism, removal of halide and attack of nucleophile takes place simultaneously
Interpretation Introduction
(c)
Interpretation: The likely mechanism of nucleophilic substitution for the given alkyl halide is to be predicted.
Concept introduction: Nucleophilic substitution reaction takes place by two mechanisms, SN1 and SN2. In SN1 mechanism, formation of carbocation takes place by removal of halide and then nucleophile attack occurs on that carbocation. However in SN2 mechanism, removal of halide and attack of nucleophile takes place simultaneously.
Interpretation Introduction
(d)
Interpretation: The likely mechanism of nucleophilic substitution for the given alkyl halide is to be predicted.
Concept introduction: Nucleophilic substitution reaction takes place by two mechanisms, SN1 and SN2. In SN1 mechanism, formation of carbocation takes place by removal of halide and then nucleophile attack occurs on that carbocation. However in SN2 mechanism, removal of halide and attack of nucleophile takes place simultaneously.
(12) Which one of the following statements about fluo-
rometry is FALSE?
a) Fluorescence is better detected at 90 from the exci-
tation direction.
b) Fluorescence is typically shifted to longer wave-
length from the excitation wavelength.
c) For most fluorescent compounds, radiation is pro-
duced by a
transition