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3.3.4 - 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 the general formula of an alkene

Back (Answer)

CnH2n

#2
Front (Question)

what elements do alkenes contain

Back (Answer)

only carbon and hydrogen atoms, making them hydrocarbons

#3
Front (Question)

what bonds do alkenes contain

Back (Answer)

alkenes contain at least one C=C double covalent bond

#4
Front (Question)

are alkenes saturated or unsaturtaed

Back (Answer)

alkenes are unsaturated

#5
Front (Question)

why are alkenes unsaturated

Back (Answer)

molecules with C=C double bonds are unsaturated as they can make more bonds with extra atoms in addition reactions

#6
Front (Question)

what feature does the C=C bond in an alkene have

Back (Answer)

as there are 2 pairs of electrons in the C=C double bond, it has a really high electron density

#7
Front (Question)

are alkenes reactive or unreactive?

Back (Answer)

alkenes are pretty reactive

#8
Front (Question)

are alkenes saturated with hydrogen?

Back (Answer)

alkenes aren’t saturated with hydrogen

#9
Front (Question)

how can double covalent bonds be formed?

Back (Answer)

by sharing 4 electrons between a pair of atoms

#10
Front (Question)

what shape do alkenes have?

Back (Answer)

alkenes have a flat planar shape

#11
Front (Question)

what is the reasoning for the shape of alkenes?

Back (Answer)

as there can be no rotation around the double bond, unlike with single bonds

#12
Front (Question)

why is there no rotation around the double bonds in alkenes?

Back (Answer)

as in addition to the single bond between the carbons, there is a p orbital (containing a single electron) on each carbon that overlap to form a pie orbital, preventing rotation of the bonds

#13
Front (Question)

what is sometimes called, when the rotation of the double bonds in alkenes is prevented?

Back (Answer)

this is sometimes called restricted rotation

#14
Front (Question)

why are alkenes reactive?

Back (Answer)

because of the double bonds which have a greater bond enthalpy, but they are an electron rich area of the molecule that can easily be attacked by positively charged electrophiles

#15
Front (Question)

why are alkenes more reactive than alkanes

Back (Answer)

carbon-carbon double bond gives the molecule an electron rich area that attracts positively charged electrophiles

#16
Front (Question)

what are electrophiles?

Back (Answer)

electron pair acceptors

#17
Front (Question)

electrophilic addition reaction: step one

Back (Answer)

positively charged electrophile is attracted towards double bond in the alkene

#18
Front (Question)

electrophilic addition reaction: step two

Back (Answer)

electrophile accepts a pair of electrons from the double bond, forming a positive ion (carbocation)

#19
Front (Question)

electrophilic addition reaction: step three

Back (Answer)

carbocation reacts with a negative ion to form a bond

#20
Front (Question)

what two types of products can from after an electrophilic addition reaction

Back (Answer)

major or minor products

#21
Front (Question)

what are major products

Back (Answer)

product that forms most of the time

#22
Front (Question)

what are minor products?

Back (Answer)

products that form less often

#23
Front (Question)

secondary carbocations

Back (Answer)

secondary carbocation is more stable as it has 2 alkyl groups, this carbocation will form most of the time

#24
Front (Question)

primary carbocations

Back (Answer)

primary carbocation is less stable as it has only 1 alkyl group, this carbocation forms less often