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Biology - 1.1, 1.2 - monomers and polymers, carbohydrates

what is a monomer?

smaller units from which larger molecules are made

what is a polymer?

molecules made from a large number of monomers joined together

give 3 examples of monomers

amino acids, monosaccharides, and nucleotides

describe a condensation reaction

joining of 2 molecules with the formation of a chemical bond and the loss of a water molecule

describe a hydrolysis reaction

the chemical bond between 2 molecules is broken and a water molecule is used

what is a monosaccharide

monomers used to make larger carbohydrates

give 3 examples of a monosaccharide

glucose, fructose, galactose

are monosaccharides water soluble

yes - they have a large number of OH groups which can form hydrogen bonds in water

what is an isomer

a different form of the same molecule

which glucose has OH above the ring

beta

which glucose has OH below the ring

alpha

how is a glycosidic bond formed

carbon 1 loses a hydrogen molecule and carbon 4 loses an OH group, causing the loss of one water molecule and the formation of an oxygen bridge (covalent)

what is maltose

alpha glucose + alpha glucose

what is sucrose

glucose + fructose

what is lactose

alpha glucose + galactose

describe the structure of glycogen (3)

highly branched every 10 monomers
condensation of alpha glucose

well compacted and stored

describe the function of glycogen

used as a carbohydrate store in animals, found in muscle and liver cells
branched structure and lots of terminal glucose means that glucose may be hydrolysed by enzymes simultaneously

where is glycogen frequent

muscle and liver cells, where rate of respiration is higher and lots of glucose is needed

describe the structure of starch

30% amylose, 70% amylopectin

describe the structure of amylose in starch

unbranched chain of glucose molecules
bonded by 1-4 glycosidic bonds

coiled and compact storing lots of energy

describe the structure of amylopectin in starch

branched chain of glucose molecules
bonded by 1-4 and 1-6 glycosidic bonds

acted on simultaneously due to frequent terminal glucose

give 3 features of starch

large and insoluble so cannot diffuse out of cells
insoluble so does not affect water potential

compact so lots stored in a given volume

describe the structure of cellulose

condensaton of beta glucose
every other monomer is inverted 180 to allow for OH group and O group to be available for 1-4 glycosidic bonding

inversion causes strong hydrogen bonds

describe the function of cellulose

long straight chains of beta glucose with strong hydrogen bonds between parallel chains creates microfibrils, main component of cell walls due to strength

do microfibrils have high tensile strength

yes - allows for the cell to be stretched without bursting from hydrostatic pressure as a result of osmosis, allowing turgidity

what are macrofibrils

collections of microfibrils
form a mesh like material used to strengthen cell walls

what bond is formed between 2 monosaccharides

glycosidic

how is a polysaccharide formed

formed by the condensation of many monomer units

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