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WorksheetsRedox Reactions
Total questions: 15
Worksheet time: 20mins
What is the furthest oxidative state for a primary alcohol?
carboxylic acid
alcohol
aldehyde
ketone
carbon dioxide
What is the furthest oxidative state for a secondary alcohol?
carboxylic acid
alcohol (no change)
carbon dioxide
ketone
aldehyde
What is the furthest oxidative state for a tertiary alcohol?
carboxylic acid
alcohol (no change)
carbon dioxide
ketone
aldehyde
Which of the following would oxidize an aldehyde to a carboxylic acid?
PCC
O3 / (CH3)2S
KMnO4
OsO4
The production of a diol using OsO4 would result in a/an ___.
syn addition
anti addition
Markovnikov product
Anti-Markovnikov product
Which of the following reagents would result in a TRANS alkene for the reduction of the alkyne shown here?
H2 / Lindler Catalyst
H2 /Pt
NH3 / Na
Which of the following reagents would result in a CIS alkene for the reduction of the alkyne shown here?
H2 / Lindler Catalyst
H2 /Pt
NH3 / Na
Which of the following reagents would result in an alkane for the reduction of the alkyne shown here?
H2 / Lindler Catalyst
H2 /Pt
NH3 / Na
How many products would result from the oxidative cleavage of this compound?
1
2
3
4
5
How many products would result from the oxidative cleavage of this compound?
1
2
3
4
5
The following molecule is treated with O3 followed by KMnO4 . The resulting product would contain which functional group(s)? Choose all that apply.
aldehyde
carboxylic acid
ketone
alcohol
ester
Draw the product of the following reaction.
Draw the original alkene.
Which reagent would be best for the selective reduction of an aldehyde?
NaBH4
LiAlH4
OsO4
H2 / Lindlar Catalyst
The increasing of bonds to a more electronegative atom (ex. oxygen) is called
(a)
