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Carbohydrates

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Total cards: 24•Content version: v4•Public deck•Updated: 8/1/2026

Card preview (24)

#1
Front (Question)

what are the functions of carbohydrates

Back (Answer)

energy and carbon source energy store flavouring functional ingredient (gum, probiotics)

#2
Front (Question)

what are the 4 types of carbohydrate

Back (Answer)

monosaccharide disaccharide oligosacchardie polysaccharides

#3
Front (Question)

outline the characteristics of monosaccharides

Back (Answer)

• simple, one sugar unit • C3H6O3 • aldoses and ketoses

#4
Front (Question)

what are the characteristics of aldoses

Back (Answer)

has a carbon and a double bonded oxygen at the end of the chain contains an aldehyde group

#5
Front (Question)

what are the characteristics of ketoses

Back (Answer)

has a carbon and double bonded oxygen in the middle of the chain contains a ketone group

#6
Front (Question)

define chiral

Back (Answer)

cannot be placed on top of its mirror image

#7
Front (Question)

examples of stereoisomers

Back (Answer)

D-… L-…

#8
Front (Question)

what are the two chiral forms

Back (Answer)

enantiomers epimers

#9
Front (Question)

what is an enantiomer

Back (Answer)

mirror reflection compounds related by inverting the configuration at all asymmetric carbons OH group pointing left = L-glucose OH group pointing right= D-glucose

#10
Front (Question)

what is an epimer

Back (Answer)

disastereomers with an inverted configuration at one asymmetric carbon

#11
Front (Question)

what is a disastereomer

Back (Answer)

compounds related by inverting configuration at one or more chiral centres

#12
Front (Question)

what is meant by the cyclic structure of monosaccharides

Back (Answer)

reaction occurs between -OH at C-5 and the aldehyde at C-1, producing a pyranose ring this produces an new asymmetric centre at C1, with two new alpha and beta stereoisomers- called anomers alpha anomer- above the ring beta anomer- below the ring the anomie’s are interchangeable by mutarotation

#13
Front (Question)

give an example of a reducing sugar

Back (Answer)

all monosaccharides glucose, fructose maltose, lactose

#14
Front (Question)

give examples of naturally occurring food monosaccharides

Back (Answer)

glucose, fructose, lactose, ribose

#15
Front (Question)

how is the anomeric carbon configuration determined

Back (Answer)

glucose • CH2OH and OH are on opposite sides on the anomeric carbon • 6 membered ring= pyranose fructose • CHOH and OH are on the same side of the anomeric carbon • 5 membered ring= furanose

#16
Front (Question)

example of a disaccharide

Back (Answer)

maltose

#17
Front (Question)

how are disaccharides formed

Back (Answer)

the hemiacetal end is free to open or close the hemiacetal group of the alpha-delta-glucose reacts with the OH group of the beta-delta-glucose and forms a glycosidic bond two monosaccharides formed by the glycosidic bond

#18
Front (Question)

how is sucrose formed

Back (Answer)

glucose and fructose = sucrose head to head no free anomeric carbon so is non-reducing inversion on heating made by plants

#19
Front (Question)

sugar beet is…

Back (Answer)

UK grown and processed in 6 factories seasonal (Sept- March)

#20
Front (Question)

sugar cane is…

Back (Answer)

a tropical plant that is shipped raw to the UK processed all year in 1 UK factory has many uses (flavour, colour, sweetener)

#21
Front (Question)

how is lactose made

Back (Answer)

glucose and galactose head to tail reducing sugar

#22
Front (Question)

give an example of a non-reading sugar

Back (Answer)

sucrose, trehalose

#23
Front (Question)

how is trehalose made

Back (Answer)

glucose and glucose head to head energy storage in insects non-reducing sugar

#24
Front (Question)

what are polyols

Back (Answer)

sugar alcohols