Basic concepts of organic chemistry Flashcards

1
Q

Saturated

A

Containing single bonds only

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2
Q

Unsaturated

A

Containing a multiple carbon-carbon bond

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3
Q

Homologous series

A

A family of compounds with similar chemical properties, whose successive members differ by the addition of a —CH2— group

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4
Q

Functional group

A

The part of the organic molecule largely responsible for the molecule’s chemical properties

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5
Q

Aliphatic

A

Carbon atoms are joined to each other in unbranched (straight) or branched chains, or non-aromatic rings

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6
Q

Alicyclic

A

Carbon atoms are joined to each other in ring (cyclic) structures, with or without branches

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7
Q

Aromatic

A

Some or all of the carbon atoms are found in a benzene ring

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8
Q

Molecular formula

A

Shows the number and type of atoms of each element present in a molecule

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9
Q

Empirical formula

A

Simplest whole number ratio of the atoms of each element present in a compound

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10
Q

General formula

A

Simplest algebraic formula for any member of a homologous series

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11
Q

Displayed formula

A

Shows the relative positioning of all the atoms in a molecule and the bonds between them

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12
Q

Structural formula

A

Shows clearly which groups are bonded together e.g. CH3(CH2)2CH3

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13
Q

Skeletal formula

A

Simplified organic formula, where all the Cs and Hs are removed and only the bonds between Cs and any functional groups are shown

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14
Q

Structural isomerism

A

Compounds with the same molecular formula but different structural formulae

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15
Q

Homolytic fission

A

Each of the bonded atoms take one of the shared pair of electrons from the bond, forming two radicals with an unpaired electron; represented using fish hook arrows

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16
Q

Heterolytic fission

A

One of the bonded atoms takes both of the electrons from the bond, forming one +ve and one -ve ion; represented using curly arrows

17
Q

Addition reaction

A

Two reactants join together to form one product

18
Q

Substitution reaction

A

An atom or group of atoms is replaced by a different atom or group of atoms; 2 reactants –> 2 products

19
Q

Elimination reaction

A

Involves the removal of a small molecule from a larger one; 1 reactant –> 2 products

20
Q

Stereoisomerism

A

Have the same structural formula but a different arrangements of atoms in space

21
Q

E/Z isomerism

A

Arises because rotation about the double bond is restricted and the groups attaches to each carbon atom are therefore fixed relative to each other (caused by pi-bond’s electron density above and below the plane of the sigma-bond)

Requires - a C=C bond and different groups attached to each of these Cs

22
Q

Cis-trans isomerism

A

Special case of E/Z isomerism, where one of the attached groups on each carbon atom of the double bond must be the same

23
Q

Effect of chain length on boiling points of alkanes

A

London forces act between molecules in close surface contact, so as chain length increase, surface area increases, allowing more surface contact; London forces will be larger

24
Q

Effect of branching on boiling point

A

Branched isomers have lower boiling points because branching means there are fewer surface points of contact between molecules (branches get in the way and prevent the molecules getting as close together as possible), resulting in fewer London forces

25
Q

Disposing of waste polymers

A

Lack of reactivity makes polymers suitable for storing food and chemicals, but also hard to dispose because they are non-biodegradable, causing environmental effects (killing marine life)

26
Q

Recycling

A

Reduces environmental impact by conserving fossil fuels and decreasing waste going to landfill.
Have to separate polymers, chop into flakes, wash, dry, then melt. Cut into pellets to use.

27
Q

PVC recycling

A

Hazardous due to high chlorine content (releases toxic gases when burnt). Used to grind before solvents were introduced, so PVC is dissolved, then recovered by precipitation.

28
Q

Using waste polymers as fuel

A

Polymers that are difficult to recycle can be incinerated to heat homes, etc. (release lots of energy due to their origin from natural gas and crude oil).

29
Q

Feedstock recycling

A

Chemical and thermal processes that can reclaim monomers, gases or oils from waste polymers. Able to handle unsorted and unwashed polymers.

30
Q

Biodegradable polymers

A

Polymers made from plant starch, cellulose, plant oils and proteins can be broken down by microorganisms into water, carbon dioxide, etc.

31
Q

Photodegradable polymers

A

Contain bonds that are weakened by absorbing light to start the degradation.