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Ch13 Alkenes

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Total cards: 24•Content version: v4•Public deck•Updated: 8/1/2026

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#1
Front (Question)

What is an alkene?

Back (Answer)

Alkenes are unsaturated hydrocarbons that contain at least 1 C=C bond (functional group). Alliphatic alkenes w/ 1 = have general formula CnH2n Alkenes can be branched, cyclic and contain 1+ double bond.

#2
Front (Question)

What is an alkene?

Back (Answer)

Alkenes are unsaturated hydrocarbons that contain at least 1 C=C bond. Alliphatic alkenes w/ 1 = have general formula CnH2n Alkenes can be branched, cyclic and contain 1+ double bond.

#3
Front (Question)

Explain sigma + pi bond Explain the formation of the double bond in alkenes:

Back (Answer)

C=C double bond is comprised of a sigma bond (σ) and a pi bond (π). σ bond: formed by overlap of orbitals directly between bonding carbon atoms. π bond: formed by sideways overlap of adjacent p-orbitals above and below bonding C atom.

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#4
Front (Question)

Define Stereoisomers:

Back (Answer)

Stereoisomers are compounds with the same structural formula but different arrangement of atoms in space.

#5
Front (Question)

Why do E/Z stereoisomers occur?

Back (Answer)

E/Z isomerism around C=C arises due to the restricted rotation around double bond which fixes the group attached to each C atom in position. Rigidity of double bond due to π bon’s electron density being concentrated above and below the plane of σ bond.

#6
Front (Question)

What conditions permit the occurence of an E/Z isomer?

Back (Answer)

2 conditions must be met: 1. C=C double bond 2. different groups attached to each C atom of double bond.

#7
Front (Question)

Describe E/Z isomerism:

Back (Answer)

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#8
Front (Question)

Why are alkenes more reactive than alkanes?

Back (Answer)

Alkenes are more reactive because the π bond is weaker than σ bond, as π requires less energy to break. When alkenes react, π bond breaks but σ bond remains intact.

#9
Front (Question)

What kind of reaction do alkenes undergo?

Back (Answer)

Alkenes undergo electrophillic addition reactions

#10
Front (Question)

draw Describe the hydrogenation of alkenes:

Back (Answer)

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#11
Front (Question)

Describe the halogenation of alkenes:

Back (Answer)

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#12
Front (Question)

What is the test for unsaturation in alkenes?

Back (Answer)

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#13
Front (Question)

Describe the addition of hydrogen halide to alkenes:

Back (Answer)

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#14
Front (Question)

Describe the addition of hydrogen halide on unsymmetrical alkenes:

Back (Answer)

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#15
Front (Question)

Describe the hydration of alkenes:

Back (Answer)

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#16
Front (Question)

Describe the addition of steam to unsymmetrical alkenes:

Back (Answer)

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#17
Front (Question)

Define ‘Electrophiles’:

Back (Answer)

Electrophiles - electron pair acceptors. Usually + ions/molecules where one of the atoms has partial positive charge.

#18
Front (Question)

Draw the mechanism for electrophillic addition of bromine to an alkene:

Back (Answer)

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#19
Front (Question)

What is Markownikoff’s Rule of carbocation?

Back (Answer)

When an unsymmetrical alkene reacts with an unsymmetrical molecule, there are 2 possible isomeric products. 1st step of mechanism- carbocation is formed as intermediate (stage) The major product will be formed from more stable carbocation

#20
Front (Question)

What are the 3 different classifications of carbocations?

Back (Answer)

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#21
Front (Question)

Describe and explain the differing stability of carbocations:

Back (Answer)

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#22
Front (Question)

Draw the mechanism for electrophillic addition of an unsymmetrical molecule to an unsymmetrical alkene:

Back (Answer)

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#23
Front (Question)

What is addition polymerisation?

Back (Answer)

• Polymerisation is carried out at high temperatures and pressures using catalysts. • A polymer is a large molecule formed from many thousands of repeat units of smaller molecules known as monomers. • Place bracket around one unit and add ‘n’ next to it for repeating units.

#24
Front (Question)

What is the structure and different uses of Poly(ethene)

Back (Answer)

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