Draw the organic products formed when cyclopentene is treated with each reagent. With some
reagents, no reaction occurs.
a.
b.
c.
d.
e.
f.
g.
h.
i.
j.
k.
l. Product in (k);
(a)
Interpretation: The organic product formed when cyclopentene is treated with
Concept introduction: The addition of
Answer to Problem 12.38P
The organic product formed when cyclopentene
Explanation of Solution
In the given reaction, when cyclopentene is treated with
Figure 1
The organic product formed when cyclopentene
(b)
Interpretation: The organic product formed when cyclopentene is treated with Lindlar catalyst is to be predicted.
Concept introduction: The addition of
Answer to Problem 12.38P
Cyclopentene do not react with Lindlar catalyst.
Explanation of Solution
Alkenes do not react with Lindlar catalyst. Lindlar catalyst is used to reduce alkynes to
Cyclopentene do not react with Lindlar catalyst.
(c)
Interpretation: The product formed when the cyclopentene is treated with
Concept introduction: In presence of sodium metal in ammonia, the is alkyne is reduced to
Answer to Problem 12.38P
Cyclopentene do not react with
Explanation of Solution
Alkenes do not react with
Cyclopentene do not react with
(d)
Interpretation: The product formed when cyclopentene is treated with
Concept introduction: In presence of peroxide, alkene is oxidized to epoxide. This is known as epoxidation. This is a syn addition. The weak pi bond of alkene and weak
Answer to Problem 12.38P
The product formed when cyclopentene is treated with
Explanation of Solution
In the given reaction, when cyclopentene is treated with
Figure 2
The product formed when cyclopentene is treated with
(e)
Interpretation: The product formed when cyclopentene is treated with
Concept introduction: Anti-dihroxylation takes place in two steps epoxidation followed by hydrolysis. In presence of peroxide, alkene is oxidized to epoxide. This is known as epoxidation. This is a syn addition. The weak pi bond of alkene and weak
Answer to Problem 12.38P
The product formed when cyclopentene is treated with
Explanation of Solution
In the given reaction, when cyclopentene is treated with
Figure 3
The product formed when cyclopentene is treated with
(f)
Interpretation: The product formed when cyclopentene is treated with
Concept introduction: Addition of two hydroxyl groups on double bond to form
Answer to Problem 12.38P
The product formed when cyclopentene is treated with
Explanation of Solution
In the given reaction, when cyclopentene is treated with
Figure 4
The product formed when cyclopentene is treated with
(g)
Interpretation: The product formed when cyclopentene is treated with
Concept introduction: Addition of two hydroxyl groups on double bond to form
Answer to Problem 12.38P
The product formed when cyclopentene is treated with
Explanation of Solution
In the given reaction, when cyclopentene is treated with
Figure 5
The product formed when cyclopentene is treated with
(h)
Interpretation: The product formed when cyclopentene is treated with
Concept introduction: The metal hydride reagents are good reducing agents such as
Answer to Problem 12.38P
Cyclopentene gives no reaction with
Explanation of Solution
The
Cyclopentene gives no reaction with
(i)
Interpretation: The product formed when cyclopentene is treated with
Concept introduction: In presence of ozone and
Answer to Problem 12.38P
The product formed when cyclopentene is treated with
Explanation of Solution
In the given reaction, when cyclopentene is treated with
Figure 6
The product formed when cyclopentene is treated with
(j)
Interpretation: The product formed when cyclopentene is treated with
Concept introduction: Sharpless epoxidation involves the oxidation of double bond between carbon atoms to epoxide. This oxidation occurs only in allylic alcohol. This is an enantioselective oxidation, which means predominantly one enantiomer is formed. Sharpless reagents are
Answer to Problem 12.38P
The product formed when cyclopenteneis treated with
Explanation of Solution
There are two different chiral diethyl tartrate isomers,
When epoxidation is done using
Figure 7
The product formed when cyclopenteneis treated with
(k)
Interpretation: The product formed when cyclopentene is treated with
Concept introduction: In presence of peroxide alkene is oxidized to epoxide this is known as epoxidation. This is a syn addition. The weak pi bond of alkene and weak
Answer to Problem 12.38P
The product formed when cyclopentene is treated with
Explanation of Solution
In the given reaction, when cyclopentene is treated with
Figure 8
The product formed when cyclopentene is treated with
(l)
Interpretation: The product formed when cyclopentene is treated with
Concept introduction: In presence of peroxide, alkene is oxidized to epoxide this is known as epoxidation. This is a syn addition. The weak pi bond of alkene and weak
Answer to Problem 12.38P
The product formed when cyclopentene is treated with
Explanation of Solution
In the given reaction, when cyclopentene is treated with
Figure 9
The product formed when cyclopentene is treated with
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