Alkanes Flashcards

1
Q

What is condensed formula?

A

Formula split into structure based parts eg CH3CH2CH2CH3 = butane

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2
Q

What is a homologous series?

A

A series of organic compounds having the same functional group but with each successive member differing by CH2

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3
Q

What is a functional group?

A

A group of atoms responsible for characteristic reactions of a compound.
Alkanes don’t have a functional group

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4
Q

What is a structural isomer?

A

A compound with the same molecular formula but a different structured formula.

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5
Q

How do you show branches in condensed formula?

A

Put them in brackets

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6
Q

How do you form the basis of the name for skeletal?

A

Number of carbons in longest chain forms base of name. E.g 5 = ending in pentane.

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7
Q

How do you show branches in name of skeletal?

A

Number of carbon it is bonded at followed by a dash and what the branch is e.g 3-methyl pentane

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8
Q

How do you show other substances branching off?

A

Short line with substance at end.

E.g of name- 2-chloropropane

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9
Q

How do you include more than one branching off in the name?

A

e.g = 2,2-dimethylpropane

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10
Q

What occurs in for example, cyclopropane?

A

A bendy ‘banana bond’

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11
Q

What is it important to remember about cyclo alkanes?

A

2 less hydrodgens (CnH2n)

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12
Q

How is alkane volatility determined and why?

A

Fewer branches = lower volatility (higher boiling point) as higher surface contact area and therefore more induced dipole-dipole forces and more energy needed to break them.
Opposite for more branches.

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13
Q

What are the 3 stages of the radical substitution method?

A

Initiation
Propagation (growing)
Termination

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14
Q

Radicals:-

A

They have an unpaired electron and are very reactive because they want to pair up

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15
Q

Initiation stage:-

A

Cl—Cl –UV–> Cl• + Cl•

Homolytic fission

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16
Q

Propagation stage:-

A

Cl• + CH4 -> •CH3 + HCl
= radical + alkane -> radical + molecule
•CH3 + Cl2 -> CH3Cl + Cl•
= alkyl radical + molecule -> molecule + free radical
Cl• is regenerated (a catalyst)
-chain reaction
-Cl• radical at the beginning is regenerated at the end so it goes back to react with more alkane molecules.

17
Q

Termination stage:-

A

Cl• + Cl• -> Cl2
•CH3 + Cl• -> CH3Cl
•CH3 + •CH3 -> C2H6

18
Q

What is displayed formula?

A

Usual (lines to show bonds)