BMS1064 - Carbohydrates Flashcards
(82 cards)
The guidelines suggest that the total carbohydrate should provide for __% of total dietary energy.
Free sugars should not exceed __% and gibre should be ___g/day.
47%
5%
30g/day
What could too much and little CHO intake lead to?
Too much: levels >75% of total energy intake have adverse effects (exclusion of protein, fat and other essential nutrients from the diet), tooth decay.
Too little: protein diverted from essential functions, CHO needed to metabolise fats, unusual products of fat breakdown (ketones) accumulate (ketosis
What are the functions of carbodhyrates?
1) Important energy and C source
2) Store energy
3) Flavouring -> react to form flavours/colours (Maillard reaction, caramelisation etc)
4) Functional incredients
- sucrose allows ice cream to be soft
- gums
- prebiotics - feed bacteria
- fat replacers
What is the difference between oligo- and polysaccharides?
Oligosaccharides = 3 to 10 monosaccharides covalently linked
Polysaccharides = >10 monosaccharides covalently linked
What is the formula for CHOs?
Cn(H2O)n
from carbon and water
CHOs are polyalcohols (C-OH). What groups do polyalcohols have?
How many carbons do the simplist sugars have? What are they structural isomers of?
Aldehyde or ketone groups
3 carbon atoms (trioses)
C3H6O3
What are the simplist members of aldehydes and ketones containing sugars called?
Aldoses and Ketoses
When is an object or molecule chiral? When is a carbon atom chiral?
If it cannot be superimposed
A carbon atom is chiral if it has 4 different groups attached. Thus they form 2 steroisomers.
What are steroisomers?
Molecules with the same molecular
formula and general structure, but with different configurations at each chiral atom
How do we count the number of C atoms in a sugar?
From the end closes to the carbonyl group
For a molecule with 3 chiral centres. How many steroistomers does it form?
2^3 = 8
2^number of chircal centres = no. of steroisomers
What are enantiomers?
Compounds related by inverting configuration at ALL chiral carbons .
Molecules that have the same molecular formula and connectivity of atoms but differ in their spatial arrangement, making them mirror-image isomers of each other.
What are diastereomers?
Compounds related by inverting configuration at ONE OR MORE, but not all chiral centres (not mirror images).
What are epimers?
Diastereomers with an inverted configuration at JUST ONE chiral carbon
All Epimers are ____1_____. But ____1____ are not epimers. Enantimomers are not ____1____. All of these are ____2____.
1 = diastereomers
2 = steroisomers
Cyclisation of glucose produces a new asymmetric centre at C-1, with the two new steroisomers called ________. These come in two forms called ____ and ____. These forms are interchangable via _________ (switching back and forth between ring and straight-chain form).
anomers
alpha and beta
mutarotation
What is the only common ketose?
Fructose - also the sweetest natural sugar.
What sugar is rare in foods in free from?
Galactose - found in milk products after lactose hydrolysis.
Whats the commonest pentose? Where is it found?
Ribose - found in meat, fish and poultry (flavour precursor)
What is the difference between furanose and pyranose forms?
Furanose - 5 membered ring
Pyranose - 6 membered ring
What is the structural difference between glucose, fructose, galactose and ribose? (two alpha, two beta / two furanoses, two pyranoses)
Ribose - alpha form
5 membered ring (furanose)
Glucose - alpa form
6 membered ring (pyranose)
Fructose - beta form
5 membered ring (furanose)
Galactose - beta form
6 membered ring (pyranose)
[All are CH2OH]
Glucose and fructose in image
Why is the structure of fructose complicated? [not needed to know]
Can form furanose and pyranose rings. Can have alpha or beta conformation.
Why is maltose (a-glucose+b-glucose) a reducing sugar?
Because it has a free anomeric carbon (a carbon bonded to 2 oxygen atoms, one of which is an -OH group (C-1) ) - and so can be oxidized.
Reducing sugars can be oxidized.
what is the difference between L and D glucose?