11.2 Nomenclature Flashcards

1
Q

What is IUPAC

A

It is the international organisation of chemists that provide the rules to name molecules so it has the same name everywhere

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2
Q

What is the root of a hydrocarbon chain

A

It is the longest continuous chain of carbons.
It is named with the prefixes

meth, eth, prop, but, pent, hex

The syllable after the root tells us if there are double bonds, eg if it is ethane there are non but if it is ethene there are.

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3
Q

What are the prefixes added for any side chains

A

Methyl,
Ethyl
Propyl
Butyl
Pentyl

So eg methylbutane means that the longest continuous carbon chain is 4 carbons, and there is a side chain of one carbon, CH3.
The branch will always have one less hydrogen.

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4
Q

How are ringed hydrocarbons named

A

They have the prefix cyclo
So eg cyclobutane etc

But they always have the same molecular formula as an alkene despite having ane suffix in their name

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5
Q

What are functional groups

A

Functional groups are a reactive group attached to the hydrocarbon chain, and this group reacts in the same way despite the length of the chain.

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6
Q

How are alcohols named

A

With the suffix ol on the end of the alkane
Eg ethanol which has functional group
CnH2n+1OH
Or just CnH2n+2O

so ethanol is C2H5OH

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7
Q

What is the difference between ketones and aldehydes

A

. Ketones have suffix one
. Aldehydes have suffix al

Eg ethanal CH3CHO
And propanone: CH3COCH3

They both have the formula of an alkane but with an oxygen added O with a double bond

However, aldehydes have the oxygen on the end of molecule, whilst ketones have the oxygen in the middle

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8
Q

Describe structure of carboxylic acids

A

End with suffix ‘oic acid’
Have a double carbon to oxygen bond

Carbon is bonded to O and OH
COOH

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9
Q

How are halogenoalkanes with more than one functional group or side chains named

A

If there are two or more halogens on a halogenoalkane, they are named in alphabetical order rather than numerical order

So eg 2-bromo-1-iodopropane
As b is before i in alphabet
And it doesn’t matter what order the numbers are in

If there are multiple of the same substituting group, use prefixes
di, tri, and tetre

Eg 1,2-dichloroethane
So there are 2 chlorines, but they are on different carbons.

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10
Q

How are numbers of functional group alcohols labelled

A

When writing alcohols, label the carbon that the OH is on by…

Butan-2-ol so put it in the middle of the word
This means the OH is on the second carbon on the chain

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11
Q

How is the number where double carbon bond is labelled on alkenes

A

In the middle of the word

So eg But-2-ene means the double bond is between the second and third carbon

Same with prop-1-ene
So double bond is between the first and second carbon

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12
Q

Describe structure of halogenoalkanes

A

In the alkane, one of the hydrogens is swapped with a halogen

no suffix, only prefix which is either
Fluoro, chloro, bromo, iodo,
And these go before the alkane

Eg 2-bromopropane

And the number of the carbon it is attached to is stated before, so the example above has the bromine on the second carbon

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13
Q

With longer carbon chains, you have to say where a side chain or functional group is located on the main chain:

How?

A

A number tells us position of any branching or functional group:

Eg methylpentane could refer to
2-methylpentane or 3-methylpentale
Because the methyl could be on the second or third carbon.
These are structural isomers

so label the carbon chain, each carbon being 1,2,3 etc.
The carbon on the side of the chain nearest to the first functional group will be labelled 1.
Because the smallest possible number is always used

So 1-bromopropane and
3-bromopropane are the same, however there is no such thing as 3-bromopropane because the smallest possible number of carbons is used.

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14
Q

What is a homologous series

A

A family of organic compounds with the same functional group, but different carbon chain lengths.

. They all have the same general formula eg CnH2n+2 for alkanes
. Each member of the series differs from the next by CH2

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15
Q

How does the length of the carbon chain affect chemical reactivity, and physical properties of the molecule

A

. The length of carbon chain has little effect on the reactivity of functional group

. However it affects physical properties..
Eg longer the chain, higher the boiling point because there are more van der walls due to more electrons in longer chains

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16
Q

Does branching affect physical properties of hydrocarbons?

A

Yes, the more branches the lower the melting and boiling points because the molecules can’t pack closely together easily