Cis-Trans Isomerism in Alkene

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This flashcard is used as revision materials after students learnt about Cis-Trans isomer in alkene.

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12 Terms

1
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What structural feature of alkenes is the reason for cis-trans isomerism?

The lack of rotation around the carbon-carbon double bond.

2
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The carbon atoms involved in a double bond that exhibits cis-trans isomerism have what type of hybridization?

sp2 hybridization.

3
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In the context of alkene isomerism, what does the prefix 'cis-' signify about the positions of substituent groups?

It signifies that the substituent groups are on the same side of the carbon-carbon double bond.

4
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In the context of alkene isomerism, what does the prefix 'trans-' signify about the positions of substituent groups?

It signifies that the substituent groups are on opposite sides of the carbon-carbon double bond.

5
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What is the specific IUPAC name for the isomer of butene where both methyl groups are on the same side of the double bond?

cis-2-butene.

6
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In (E)-3-methyl-1,3-pentadiene, are the higher-priority groups on the relevant double bond on the same side or opposite sides?

They are on opposite sides, which is why it is designated E (entgegen).

7
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The letter 'Z' in the E-Z system is derived from the German word zusammen, which means what?

Together.

8
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The priority of each substituent in the E-Z system is determined by following the Cahn-Ingold-_____ (CIP) system.

Prelog

9
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What is the name of the system that uses a set of sequence rules to assign priorities to substituent groups on double bond carbons?

The E-Z system.

10
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The letter 'E' in the E-Z system is derived from the German word entgegen, which means what?

Opposite.

11
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What is the specific IUPAC name for the isomer of butene where the methyl groups are on opposite sides of the double bond?

trans-2-butene.

12
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In (Z)-2-hydroxymethyl-2-butenoic acid, are the higher-priority groups (-COOH and -H22OH) on the same side or opposite sides of the double bond?

They are on the same side, which is why it is designated Z (zusammen).