intro to carbohydrates and lipids Flashcards
what are the key structures of linear monosaccharides
- hydroxyl group (-OH)
- carbonyl group - aldehyde (-CHO) or ketone (-C=O)
names for number of carbon atoms 3-7
3- triose
4- tetrose
5- pentose
6- hexose
7- heptose
what are reducing sugars
- when carbonyl groups (aldehyde or ketone) can react to gain oxygen
- sugar is oxidised while another compound is reduced
draw the mechanism for a reducing sugar and Benedict reagent
HRC=O + Cu(citrate)2 -2 + Cu2+——> -ORC=O + Cu2O(s)
how do linear monosaccharides go from linear to rings
in an aqueous solution aldehydes or ketones react with hydroxyl on a carbon further along forming a ring structure
what ring structures do aldehyde and ketones produce when forming basic rings
aldehyde + alcohol <—–> hemiacetal
ketone + alcohol <——> hemiketal
what is a chiral carbon
- asymetircial
- 4 different groups attached
- arranged to produced isomers
what is a L isomer of a carbohydrate
-OH on terminal carbon ( second to last) is on the left side
what is a D isomer of a carbohydrate
-OH on terminal carbon (second to last) is on the right side
what is a constitutional isomer
different order of attachment of atoms
what is a sterioisomer
atoms are connected in the same order but differing spacial arrangement
what is an enantiomer
mirror images
what are diastereoisomers
isomers that are not mirror images
what are epimers
differ at one of the several asymmetric carbon atoms
what are anomers
differ at a new asymmetric carbon atom formed on a ring closure
when glucose is in equilibria how many parts of each anomer is present
1/3 - alpha
2/3 - beta
what are the naturally occurring links in disaccharides
1-4, 1-6, 1-2