Biological Molecules: Carbohydrates Flashcards

1
Q

what are some examples of reducing sugars

A

all monosaccharides and maltose

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2
Q

why are carbohydrates, proteins and lipids all organic compounds

A

they contain the elements Carbon and Hydrogen

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3
Q

why are carbon atoms key to the organic compounds

A
  • each carbon atom can form four covalent bonds which makes the compounds very stable (as covalent bonds are very strong and so require a large amount of energy to break them)
  • they can form covalent bonds with oxygen, nitrogen and sulfur
  • they can bond to form straight chains, branched chains or rings
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4
Q

what are macromolecules

A

very large molecules that contain 1000 or more atoms and therefore having a high molecular mass

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5
Q

difference between macromolecules and polymers

A

polymers can be macromolecules but not all macromolecules are polymers as the subunits of polymers have to be the same repeating units

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6
Q

what is the general formula for carbohydrates

A

Cx(H20)y

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7
Q

what are the three types of carbohydrates

A
  • monosaccharides, disaccharides and polysaccharides
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8
Q

definition of a monosaccharide

A
  • single sugar monomer
    (all are reducing sugars)
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9
Q

definition of a disaccharide

A

a sugar formed from two monosaccharides joined by a glycosidic bond

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10
Q

definition of a polysaccharide

A

a polymer formed by many monosaccharides joined by glycosidic bonds

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11
Q

what is maltose made up of

A

two alpha glucose molecules

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12
Q

what is sucrose made out of

A

an alpha glucose and a fructose molecule

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13
Q

what monomers is cellulose made out of

A

beta glucose

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14
Q

what monomers is starch made out of

A

alpha glucose in the form of amylose and amylopectin

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15
Q

what monomers is glycogen made out of

A

alpha glucose

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16
Q

how many carbons in a glyceraldehyde molecule

A

3

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17
Q

how many carbons in a ribose molecule

A

5

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18
Q

how many carbons in a glucose

A

6

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19
Q

are lipid molecules polymers

A

no because each fatty acid joins to a glycerol molecule rather than to each other

also separate molecules (such as triglycerides) are not held together by covalent bonds so they cannot be classed as polymers

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20
Q

what are the two types of covalent bonds

A

nonpolar - when the electrons are shared equally
or
polar - where the electrons are shared unequally due to an electronegative atom

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21
Q

what is a condensation reaction

A

when monomers combine together by covalent bonds accompanied by the release of a water molecule

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22
Q

how do you reverse a condensation reaction

A

using hydrolysis (add water and break the bonds)

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23
Q

what covalent bonds exist within carbohydrates ????

A

glycosidic bonds

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24
Q

what covalent bonds exist within lipids ?????

A

esters

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25
what covalent bonds exist within nucleic acids ?????
phosphodiester
26
what is a reducing sugar
a sugar that can donate electrons (its carbonyl group becomes oxidised) -> the sugar becomes the reducing agent
27
why can reducing sugars be detected using Benedict's solution
they reduce the soluble copper sulphate to insoluble (brick-red) copper oxide
28
what are some examples of reducing sugars
all monosaccharides and maltose
29
how are glucose, fructose and galactose linked
they all have the same molecular formula but have a different structural formula the different arrangements of atoms in them gives them slightly different properties
30
how can we adapt the Benedict's solution to detect non-reducing sugars
they must first be hydrolysed (heat it with acid) to break the disaccharide into its two monosaccharides
31
what is a triose
a monosaccharide formed from 3 carbon atoms
32
structure of alpha glucose
H H OH OH
33
structure of beta glucose
H OH OH H
34
why are monosaccharides bonded together to form disaccharides and polysaccharides in cells
- so they are more suitable for transport and storage - so they have less influence of a cell's osmolarity
35
how are di- and poly-saccharides formed
when two hydroxyl groups on different saccharides interact to form a strong covalent bonds call a glycosidic bond
36
how are two alpha glucose molecules joined to form a disaccharide
the OH groups are affected on the ends: the OH of one is removed and the H from the OH of the other is removed 1st picture from 1.1.5 the glycosidic bond
37
how do glycosidic bonds find the energy to form between saccharides
they are catalysed by enzymes specific to which OH groups are interacting
38
what type of glycosidic bonds does maltose have
- alpha 1,4
39
what type of glycosidic bonds does sucrose have
alpha 1,2
40
what type of glycosidic bonds does cellulose have
beta 1,4
41
what type of glycosidic bond does amylose have
alpha 1,4
42
what type of glycosidic bond does amylopectin have
alpha 1,4 and 1,6
43
what are some examples of hydrolytic (hydrolysis) reactions
- the digestion of food in the alimentary tract - the breakdown of stored carbohydrates in muscle and liver cells for use in cellular respiration
44
what type of sugar is sucrose
non-reducing
45
how do we prove sucrose is a non-reducing sugar
- benedict's test - negative result - heat with (hydrochloric) acid - benedict's test - positive result
46
why does a non-reducing sugar give a positive result after it has been heated in acid
the heating with acid provides the water that hydrolyses the glycosidic bond resulting in two monosaccharides which are reducing sugars
47
what is a glycosidic bond
a strong covalent bond with an oxygen link that results from the interaction between two hydroxyl groups
48
how do we make polysaccharides into monosaccharides
through MANY hydrolysis reactions
49
what two phases do all chromatography techniques use
- mobile phase - stationary phase
50
1.1.6 chromatography: monosaccharides
51
what chemical bond forms between monosaccharides
glycosidic bond
52
how to calculate the chemical formula of a disaccharide using the formulas of two monosaccharides
- add all the carbons, hydrogens and oxygens of both monomers then subtract 2H and 1O (the water molecule lost)
53
what are three common disaccharides
- maltose - sucrose - lactose
54
what monosaccharides is maltose made out of
alpha glucose and alpha glucose
55
what monosaccharides is sucrose made out of
alpha glucose and fructose
56
what monosaccharides is lactose made out of
alpha glucose and galactose
57
what are three common monosaccharides
- glucose - galactose - fructose
58
why are starch and glycogen good storage molecules
- compact (so large quantities can be stored) - insoluble (so will have no osmotic effect)
59
where and how is starch stored in plants
stored as granules in plastids
60
what two polysaccharides is starch made out of and what percentage composition are they
- amylose (10-30%) - amylopectin (70-90%)
61
what is the structure of amylose
- 1,4 glycosidic bonds between alpha glucose - which creates an unbranched molecule
62
between starch and glycogen, which is quicker to be broken down and why
glycogen because it is more branched which means more enzymes can work on it simultaneously on the many terminal glucose molecules
62
why does 'being branched' help a polymer be broken down quicker
it enables more free ends where glucose molecules can be removed [or added] (more enzymes can work simultaneously) allowing for hydrolysis [or condensation] reactions to occur more rapidly
62
what is the structure of amylopectin
- 1,4 and 1,6 glycosidic bonds between alpha glucose molecules - which creates a branched molecule
63
what is glycogen the storage molecule for
animals and funghi
63
why is it important that glycogen is more branched than starch
- so it is able to be broken down quicker than starch because glycogen is used as a storage molecule in animals which have a higher metabolic rate than plants (whereas starch is used as a storage molecule in plants) - so it is more compact which helps animals store more
64
where in animals has a high concentration of glycogen
in the liver and muscles as the cellular respiration rate is high in these cells