nature's chemistry Flashcards

1
Q

saturated vs unsaturated

A

saturated compounds only contain C-C single bonds, unsaturated compounds contain at least one C-C double bond.

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2
Q

how do you test for unsaturation?

A

add bromine water, if the compound is unsaturated then it will quickly decolourise

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3
Q

what is an isomer?

A

compounds with the same molecular formula but different structural formulas

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4
Q

what is the functional group in alcohols called?

A

hydroxyl (OH)

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5
Q

primary, secondary and tertiary alcohols

A

primary: carbon attached to the functional group is only attached to one other carbon
secondary: carbon attached to the functional group is attached to two other carbons
tertiary: carbon attached to the functional group is attached to three other carbons

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6
Q

diols and triols

A

diol: alcohols with two OH groups
triol: alcohols with three OH groups

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7
Q

how does number of hydroxyl groups affect the alcohols?

A

more hydroxyl groups will result in a higher melting and boiling point due to the greater degree of hydrogen bonding.

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8
Q

what is the functional group in a carboxylic acid called?

A

carboxyl (COOH)

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9
Q

reactions that carboxylic acids have

A

+ metal oxide = salt + water
+ metal hydroxide = salt + water
+ metal carbonate = salt + water + carbon dioxide

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10
Q

ester link?

A

COO

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11
Q

how are esters produced and named?

A

produced from an alcohol and carboxylic acid.
first part of the name comes from alcohol, the second from the carboxylic acid e.g. ethanol + propanoic acid = ethyl propanoate

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12
Q

uses of esters

A

flavourings, fragrances, solvents

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13
Q

reactions to form and break esters

A

condensation forms esters, hydrolysis breaks them

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14
Q

what is a condensation reaction?

A

two molecules join together to form a bigger one, with the elimination of a small molecule, usually water.

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15
Q

what is a hydrolysis reaction?

A

breaking of a large molecule by the addition of water.

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16
Q

formation of edibles fats end oils

A

they’re formed from the condensation of glycerol with 3 fatty acid chains

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17
Q

explain the difference in melting points of fats and oils

A

oils have a higher degree of unsaturation and therefore prevents the chains packing together closely, so there are fewer LDFs and therefore have a lower melting point

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18
Q

why do we need fats and oils?

A

they’re a concentrated source of energy for us and are essential for the transport and storage of fat-soluble vitamins for our bodies

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19
Q

formation of soaps

A

produced by alkaline hydrolysis of edible fats and oils, which produces 3 fatty acid molecules and glycerol. the fatty acid molecules are then neutralised by an alkali, forming ionic salts, which we call soaps.

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20
Q

use of soaps

A

to remove non-polar substances like oil and grease

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21
Q

action of soaps

A

hydrophilic polar head enters the water, leaving the hydrophobic non-polar tail in the oil/grease. agitation of the mixture causes small ball-like structures form, and the negatively charged heads repel each other, preventing them from combining. this allows the oil/grease to be removed

22
Q

hard water

A

water containing high levels of dissolved metal ions.
scum (insoluble precipitate) is commonly found in areas with hard water.

23
Q

detergents

A

do not form scum with hard water

24
Q

what do emulsifiers do?

A

prevent polar and non-polar substances from separating into layers

25
structure of emulsifiers
one or two fatty acid chains attached to glycerol
26
how emulsifiers work
there are spare hydroxyl groups, which means there is a non-polar, hydrophobic part which can dissolve in oil/grease, and a polar, hydrophilic part which can dissolve in water
27
role of proteins
major structural materials of animal tissues, essential for the maintenance and regulation of life processes
28
what are proteins made from?
amino acids
29
groups in an amino acid
an amino group (NH2) and a carboxyl group (COOH)
30
how are proteins formed?
the amino group on one amino acid and the carboxyl group of another join together, with the elimination of water (condensation reaction)
31
peptide link
CONH
32
essential amino acids
required by the body but have to obtained through the diet
33
what happens to proteins during digestion?
they're broken down via enzyme hydrolysis
34
protein shape
can form spirals, sheets, and other complex shapes. they are kept in these shapes by intermolecular (hydrogen) bonding
35
what happens to proteins when they're heated?
intermolecular bonds are broken which denatures the protein, which causes the texture of food to change
36
oxidation (ratio)
increases oxygen to hydrogen ratio
37
reduction (ratio)
reduces oxygen to hydrogen ratio
38
oxidation of alcohols
primary alcohol - aldehyde - carboxylic acid secondary alcohol - ketones cannot be oxidised tertiary alcohols cannot be oxidised
39
oxidising agents + colour changes
- hot copper oxide (black to brown) - acidified dichromate solution (orange to green) - Fehling's solution (blue to brick red) - Tollen's reagent (forms silver mirror)
40
what can oxidising agents be used to identify?
aldehydes (not ketones)
41
why can't tertiary alcohols be oxidised?
branch attched to carbon attached to hydroxyl group means =O can't be formed
42
aldehydes vs ketones
both have carbonyl groups (=O), but aldehyes have it on the end of the molecule, ketones have it in the middle
43
uses of aldehydes
have distinct flavours and aromas so are used in food products or essential oils
44
what happens when food reacts with oxygen?
oxygen from the air reacts with edible oils, giving them a rancid flavour
45
antioxidants
molecules that prevent unwanted oxidation from occurring by being oxidised in their place (they are reducing agents)
46
essential oils
concentrated extracts of volatile, non-water soluble aroma compounds which come from plants. used in perfumes, cosmetic products, flavourings, and cleaning products
47
what are terpenes made from?
isoprene units bonding together
48
effect of UV light on the body
breaks bonds, causing sunburn, ageing, and cancer
49
what is a free radical
atom/molecule that is highly reactive as it has an unpaired electron
50
steps in a chain reaction
1. initiation (free radicals on right) 2. propagation (free radicals on both sides 3. termination (free radicals on left)
51
free radical scavengers
molecules that react with free radicals to form stable molecules to prevent any unwanted chain reactions from occurring.