alkenes Flashcards

(16 cards)

1
Q

are they a class of hydrocarbons

A

yes

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

what is their general formula

A

CnH2n

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

are they saturated or unsaturated hydrocarbons

A

unsaturated

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

define an unsaturated hydrocarbon

A

the carbon atoms are not bonded to the maximum amount of hydrogen atoms possible and a C=C bond is present

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

list all the alkenes up to decene

A

methene hexene
ethene heptene
propene octene
butene nonene
pentene decene

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

draw the structural formula of dec-5-ene

A
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

draw the shortened structural formula of dec-5-ene

A
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

draw the skeletal formula of dec-5-ene

A
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

do all alkenes have straight chains

A

no, they can be branched

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

draw the branched structural formula of but-2-ene

A
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

what group does 2-methylprop-1-ene have

A

an alkyl group

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

Whats the general formula of an alkyl group

A

CnH2n+1

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

what does the 1 in 2-methylprop-1-ene represent

A

which carbon the double bond is on

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

name all the alkyl groups up to decyl

A

methyl hexyl
ethyl heptyl
propyl octyl
butyl nonyl
pentyl decyl

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

what type of reactions do alkenes take part in

A

addition reactions

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

what allows them to do this

A

reactants can add across the double bond, breaking the Pi bond but leaving the sigma bond intact