Do you know your functional group transformations from every angle? Alert - you should know these transformations well for your exams (all the way until the final exam of CH223!)
A) Select the organic starting material (in the context of our study thus far) that is used with PBr3.
alkane
alkene
primary alkyl chloride
primary alcohol
primary alkyl bromide
tertiary alkyl chloride
tertiary alkyl bromide
tertiary alcohol
B) Select the major organic product (in the context of our study thus far) that results from the use of PBr3.
alkene
primary alcohol
primary alkyl chloride
tertiary alcohol
alkane
tertiary alkyl chloride
primary alkyl bromide
tertiary alkyl bromide
C) Select the organic starting material (in the context of our study thus far) that is used with HCl.
tertiary alcohol
primary alcohol
alkane
tertiary alkyl chloride
primary alkyl chloride
alkene
primary alkyl bromide
tertiary alkyl bromide
D) Select the major organic product (in the context of our study thus far) that results from the use of HCl.
primary alkyl bromide
primary alcohol
tertiary alkyl bromide
tertiary alcohol
alkane
tertiary alkyl chloride
primary alkyl chloride
alkene
E) Select the organic starting material (in the context of our study thus far) that is used with Br2.
alkene
tertiary alcohol
tertiary alkyl bromide
tertiary alkyl chloride
alkane
primary alcohol
primary alkyl chloride
primary alkyl bromide
F) Select the major organic product (in the context of our study thus far) that results from the use of Br2.
primary alcohol
primary alkyl bromide
tertiary alkyl bromide
alkene
primary alkyl chloride
alkane
tertiary alkyl chloride
tertiary alcohol
G) Select the reagent needed for a practical reaction with an isoalkane with more than 4 carbons.
HI
HF
PBr3
I2
HCl
F2
HBr
Cl2
Br2
SOCl2, base
H) Select the major organic product resulting from reaction in part G.
primary alkyl bromide
alkane
primary alkyl chloride
tertiary alkyl bromide
alkene
primary alcohol
tertiary alcohol
tertiary alkyl chloride
I) Select the reagent needed for a practical reaction with a primary alcohol without having to heat the reaction to a high temperature.
PBr3
F2
Br2
I2
HCl
HF
Cl2
HBr
Do you know your functional group transformations from every angle? Alert - you should know these transformations well for your exams (all the way until the final exam of CH223!)
A) Select the organic starting material (in the context of our study thus far) that is used with PBr3.
alkane
alkene
primary alkyl chloride
primary alcohol
primary alkyl bromide
tertiary alkyl chloride
tertiary alkyl bromide
tertiary alcohol
B) Select the major organic product (in the context of our study thus far) that results from the use of PBr3.
alkene
primary alcohol
primary alkyl chloride
tertiary alcohol
alkane
tertiary alkyl chloride
primary alkyl bromide
tertiary alkyl bromide
C) Select the organic starting material (in the context of our study thus far) that is used with HCl.
tertiary alcohol
primary alcohol
alkane
tertiary alkyl chloride
primary alkyl chloride
alkene
primary alkyl bromide
tertiary alkyl bromide
D) Select the major organic product (in the context of our study thus far) that results from the use of HCl.
primary alkyl bromide
primary alcohol
tertiary alkyl bromide
tertiary alcohol
alkane
tertiary alkyl chloride
primary alkyl chloride
alkene
E) Select the organic starting material (in the context of our study thus far) that is used with Br2.
alkene
tertiary alcohol
tertiary alkyl bromide
tertiary alkyl chloride
alkane
primary alcohol
primary alkyl chloride
primary alkyl bromide
F) Select the major organic product (in the context of our study thus far) that results from the use of Br2.
primary alcohol
primary alkyl bromide
tertiary alkyl bromide
alkene
primary alkyl chloride
alkane
tertiary alkyl chloride
tertiary alcohol
G) Select the reagent needed for a practical reaction with an isoalkane with more than 4 carbons.
HI
HF
PBr3
I2
HCl
F2
HBr
Cl2
Br2
SOCl2, base
H) Select the major organic product resulting from reaction in part G.
primary alkyl bromide
alkane
primary alkyl chloride
tertiary alkyl bromide
alkene
primary alcohol
tertiary alcohol
tertiary alkyl chloride
I) Select the reagent needed for a practical reaction with a primary alcohol without having to heat the reaction to a high temperature.
PBr3
F2
Br2
I2
HCl
HF
Cl2
HBr
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