Alkanes Flashcards

1
Q

What type of bonding occurs in alkanes?

A
  • Sigma bonds - end to end overlap of orbitals
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

What shape is around each c atom in alkanes?

A

Tetrahedral, 109.5, 4 bonding pairs with each pair of electrons repelling equally

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

In straight chain alkanes what is the trend in boiling point and why ?

A
  • Boiling point increases as chain length increases
  • why? Induced dipole-dipole interactions get stronger as no. of electrons increases
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

Describe the trend in boiling point in branched chain alkanes + why?

A

-boiling point decreases as number of branches increases
- why? Less surface contact between chains so IDDs get weaker and need less energy to break

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

Describe reactivity in alkanes

A
  • unreactive
  • high bond enthalpies in molecules
  • low bond polarity in sigma bonds. C and H have similar electronegativities
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

Give the reaction for complete combustion of propane

A

C3H8 + 5O2 —> 3CO2 + 4H2O

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

Give the products of the incomplete combustion of an alkane and describe the problems of one product

A

CO/C and H2O
CO - toxic, reduces ability to carry O2
C(s) - soot can irritate respiratory system

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

What mechanism is used when reacting alkanes with halogens ?

A

Radical substitution

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

What needs to be present for radical sub to be able to take place?

A

Uv light

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

Describe the stages of radical substitution
(Cl)

A

Initiation - uv light breaks halogens covenant bond producing 2 chlorine radicals (homolytic fission)
Cl2 —> 2Cl*

Propagation - radical Chlorine attaches to a H from alkane chain and produces HCl
C2H6 + Cl* —> c2H5* + HCl
Radical alkane reacts with Chlorine to form haloalkane
C2H5* + Cl2 —> C2H5Cl + Cl*

Termination - two radicals combine
Cl* + Cl* —> Cl2
C2H5* + C2H5* —> C4H10
C2H5* + Cl* —> C2H5Cl

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

What would happen in radical sub if halogen was in excess?

A

Can end up with Dihalogen substance

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