(a) Interpretation: The mechanism of substitution for the given reaction and the solvent that afford the faster reaction is to be determined. 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 on that carbocation. However in S N 2 mechanism, removal of halide and attack of nucleophile takes place simultaneously. The polar protic solvent favors S N 1 reaction whereas polar aprotic solvent favors S N 2 reaction.
(a) Interpretation: The mechanism of substitution for the given reaction and the solvent that afford the faster reaction is to be determined. 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 on that carbocation. However in S N 2 mechanism, removal of halide and attack of nucleophile takes place simultaneously. The polar protic solvent favors S N 1 reaction whereas polar aprotic solvent favors S N 2 reaction.
Solution Summary: The author explains the mechanism of substitution for the given reaction and the solvent that affords the faster reaction.
Definition Definition Solvents that are chemically polar in nature and are not capable of hydrogen bonding. Some commonly used polar aprotic solvents are acetone, DMF, acetonitrile, and DMSO.
Chapter 7, Problem 7.37P
Interpretation Introduction
(a)
Interpretation: The mechanism of substitution for the given reaction and the solvent that afford the faster reaction is to be determined.
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 on that carbocation. However in SN2 mechanism, removal of halide and attack of nucleophile takes place simultaneously. The polar protic solvent favors SN1 reaction whereas polar aprotic solvent favors SN2 reaction.
Interpretation Introduction
(b)
Interpretation: The mechanism of substitution for the given reaction and the solvent that afford the faster reaction is to be determined.
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 on that carbocation. However in SN2 mechanism, removal of halide and attack of nucleophile takes place simultaneously. The polar protic solvent favors SN1 reaction whereas polar aprotic solvent favors SN2 reaction.
Interpretation Introduction
(c)
Interpretation: The mechanism of substitution for the given reaction and the solvent that afford the faster reaction is to be determined.
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 on that carbocation. However in SN2 mechanism, removal of halide and attack of nucleophile takes place simultaneously. The polar protic solvent favors SN1 reaction whereas polar aprotic solvent favors SN2 reaction.
These are in the wrong boxes. Why does the one on the left have a lower molar mass than the one on the right?
SYNTHESIS REACTIONS. For the following reactions, synthesize the given products from the given reactants.
Multiple reactions/steps will be needed. For the one of the steps (ie reactions) in each synthesis, write out the
mechanism for that reaction and draw an energy diagram showing the correct number of hills and valleys for
that step's mechanism.
CI
b.
a.
Use acetylene (ethyne)
and any alkyl halide as
your starting materials
Br
C.
d.
"OH
OH
III.
OH
Calculate the pH and the pOH of each of the following solutions at 25 °C for which the substances ionize completely:
(a) 0.200 M HCl