4.1 - basic concepts and hydrocarbons Flashcards

1
Q

What is nomenclature?

A

The system of naming compounds

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2
Q

Hydrocarbons are made up of molecules that contain only hydrogen and carbon atoms. When you look at their structures, you can classify them as: (give 3 classifications and their definitions)

A
  • aliphatic hydrocarbons: in which the carbon atoms are joined together in either straight (unbranched) chains or branched chains
  • alicyclic hydrocarbons: in which the carbon atoms are joined together in a ring structure but are not aromatic
  • aromatic hydrocarbons: in which there is at least one benzene ring in the structure
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3
Q

Define homologous series

A

A homologous series is a series of organic compounds that have the same functional group with successive members differing by CH2

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4
Q

Give the first ten prefixes of alkanes and alkenes

A

1) meth
2) eth
3) prop
4) but
5) pent
6) hex
7) hept
8) oct
9) non
10) dec

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5
Q

What are alkanes?

A

The simplest homologous series is the alkanes. They are aliphatic saturated hydrocarbons, so they contain only carbon and hydrogen joined by single covalent bonds.

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6
Q

What three rules do you need to consider when naming an organic compound?

A

stem - the main part of the name; generated by identifying the longest carbon chain or parent chain

suffix - the end of the name; identifies the most important functional group

prefix - the front part of the name; identifies the other functional groups and the carbon atoms they are attached to

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7
Q

Name the first ten alkyl groups (these are known as the stem)

A

1) methyl
2) ethyl
3) propyl
4) butyl
5) pentyl
6) hexyl
7) heptyl
8) octyl
9) nonyl
10) decyl

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8
Q

Define a saturated compound

A

Saturated compounds have only single bonds

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9
Q

Define functional group

A

A functional group is a group of atoms that is responsible for the characteristic chemical reactions of a compound

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10
Q

What four things should you remember when naming compounds?

A

1) numbers are used to indicate which carbon atom an alkyl group is joined to
2) dashes are used to separate numbers from words
3) commas are used to separate numbers
4) prefixes are written in alphabetical order using the smallest numbers possible to indicate which carbon atoms they are joined to

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11
Q

No number is needed when naming aldehydes because this functional group is always on a terminal (end) carbon atom. For organic compounds with more than one identical group, add…

A
  • ‘di-‘ to show two of the same group
  • ‘tri-‘ to indicate three of the same group
  • ‘tetra-‘ to describe four identical groups
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12
Q

What is the general formula of alkanes?

A

CnH2n+2

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13
Q

Define general formula

A

A general formula is the simplest algebraic formula for a homologous series

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14
Q

Define display formula

A

A displayed formula shows the relative positions of atoms and the bonds between them

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15
Q

Define structural formula

A

A structural formula provides the minimum detail for the arrangement of atoms in a molecule

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16
Q

What five steps can you use to work out the empirical formula?

A

1) change the percentages to masses
2) calculate the number of moles in each element using: amount in moles = mass/RFM
3) divide by the smallest value
4) change the ratio to whole numbers
5) write the formula

17
Q

You can use a three-step method to generate the molecular formula from the empirical formula and molecular mass. What are these three steps?

A

1) calculate the relative empirical mass using the empirical formula
2) divide the relative molecular mass by the empirical formula mass
3) multiply each atom in the empirical formula by the number calculated in step 2 and write the molecular formula

18
Q

Define skeletal formula

A

a skeletal formula is a simplified structural formula drawn by removing hydrogen atoms from alkyl chains

19
Q

Define unsaturated

A

Unsaturated organic chemicals contain at least one carbon-carbon double covalent bond

20
Q

Define structural isomer

A

Structural isomers are compounds with the same molecular formula but different structural formulae

21
Q

Define stereoisomers

A

Stereoisomers are organic compounds with the same molecular formula and structural formula but having a different arrangement of atoms in space

22
Q

Define Cis-trans isomerism

A

Cis-trans isomerism is a type of E/Z isomerism in which the two substituent groups attached to both carbon atoms of the C=C bond are the same

23
Q

Define E/Z isomerism

A

E/Z isomerism is a type of steeoisomerism caused by the restricted rotation around the double bond -two different groups are attached to both carbon atoms of the C=C double bond

24
Q

Structural isomers are compounds with the same molecular formula but different structural formula. In what three ways can this happen?

A
  • the alkyl groups are in different places
  • the functional group can be bonded to different parts of the parent chain
  • the functional group could be different
25
Q

Define reaction mechanisms

A

Reaction mechanisms are the models that show the movement of electron pairs during a reaction

26
Q

Define curly arrows

A

Curly arrows model the flow of electron pairs during reaction mechanisms

27
Q

Define homolytic fission

A

Homolytic fission happens when each bonding atom receives one electron from the bonded pair, forming two radicals

28
Q

Define radicals

A

Radicals are species with one or more unpaired electrons

29
Q

Define heterolytic fission

A

Heterolytic fission happens when one bonding atom receives both electrons from the bonding pair

30
Q

What happens in the initiation step and what conditions are required?

A

A free radical is created.

UV light or temperatures of about 300 degrees C are needed