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Alkenes

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Total cards: 24•Content version: v3•Public deck•Updated: 8/1/2026

Card preview (24)

#1
Front (Question)

What is an alkene?

Back (Answer)

An unsaturated hydrocarbon.

#2
Front (Question)

What is a hydrocarbon?

Back (Answer)

A compound containing hydrogen and carbon atoms only.

#3
Front (Question)

What does unsaturated mean?

Back (Answer)

Contains one or more C=C double bonds.

#4
Front (Question)

What is the general formula of alkenes with one double bond?

Back (Answer)

CnH2n

#5
Front (Question)

How do you determine the root name of an alkene?

Back (Answer)

Find largest carbon change (eth-, prop- ect)

#6
Front (Question)

How should the carbon chain be numbered in alkenes?

Back (Answer)

So the double bond has the lowest possible number.

#7
Front (Question)

How is the position of the double bond shown in the name?

Back (Answer)

Number placed in the middle with dashes e.g pent-2-ene

#8
Front (Question)

How are branches or halogens shown in alkene names?

Back (Answer)

Numbered and added as prefixes in alphabetical order.

#9
Front (Question)

What is the priority order of functional groups (lowest to highest)?

Back (Answer)

Halogens –> Alkyl groups –> Alkenes –> Others

#10
Front (Question)

What intermolecular forces exist between alkene molecules?

Back (Answer)

Van der Waals forces only.

#11
Front (Question)

How do alkene physical properties compare to alkanes?

Back (Answer)

Very similar to equivalent alkanes.

#12
Front (Question)

How does melting/boiling point change with chain length?

Back (Answer)

Increases as chain length increases (stronger Van der Waals).

#13
Front (Question)

Are alkenes soluble in water?

Back (Answer)

No.

#14
Front (Question)

Why are alkenes more reactive than alkanes?

Back (Answer)

They are unsaturated and can undergo addition reactions.

#15
Front (Question)

Why are alkenes susceptible to electrophiles?

Back (Answer)

The C=C has high electron density (pi bond)

#16
Front (Question)

What type of combustion do alkenes undergo?

Back (Answer)

Combustion like hydrocarbons.

#17
Front (Question)

Why are alkenes rarely used as fuels?

Back (Answer)

Likely incomplete combustion so less energy and more CO or C formed.

#18
Front (Question)

Why are alkenes useful in synthesis?

Back (Answer)

They undergo many reactions and act as starting molecules.

#19
Front (Question)

What is the bond angle around a C=C double bond?

Back (Answer)

Planar with bond angles of around 120 degrees.

#20
Front (Question)

In larger alkenes which part is planar?

Back (Answer)

Only the C=C unit.

#21
Front (Question)

Can C=C bonds rotate?

Back (Answer)

No they are rigid.

#22
Front (Question)

What makes up a C=C double bond?

Back (Answer)

One sigma bond and one pi bond.

#23
Front (Question)

How is the sigma bond formed?

Back (Answer)

Overlap of 2s orbitals.

#24
Front (Question)

How is the pi bond formed?

Back (Answer)

Overlap of p orbitals and below the plane.