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Saccharides = sugar ends in - |
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a sugar that is a smal CHO. -ose |
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Example of naming a 5 and 6 C sugar |
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pentose=ribose Hexose- glucose, fructose |
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Glyceraldehyde is -- where dihydroxyacetone is not-- |
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Fischer projection of glyceraldehyde |
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Glucose- # of C and OH Aldehyde or Ketone? Numbering starts on- |
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Aldehyde 6C 5OH starts with C on Aldehyde |
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Fructose aldehyde or ketone? #C how numbering starts? |
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Ketone 6C Numbering starts with ketone where the aldehyde would be |
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Determining D or L
ex: glucose/fructose |
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Go to the furthest C from the aldehyde and compare it to glyceraldehyde to find if D or L. This is the chiral carbon so in glucose or fructose it would be C5 not C6 bc 6 isnt chiral |
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Aldehydes and Ketones react with-- to make hemiacetals or hemiketals which can react with -- to make an acetal which creats a -- at -- which produces -- |
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alcohol another alcohol New chiral center at carbonyl carbon produces glycosidic bond |
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When is the chiral carbon introduced? |
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NucleoSides are the dehydration prodct of -- |
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pyrimidine or purine with the sugar (deoxy or ribose) Do not have phosphate! |
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adding a phosphate group to the nucleoside |
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Phosphate groups bind at #C? |
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Phosporyl= -PO3H -2 Phosphate= HO-PO3H +2 |
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Hydrolysis of ATP in terms of which phosphate is removed. Why? |
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Gamma is furthers P from the sugar. Beta is 2nd. These are highly exorgenic and is coupled to endergonic rxns in the cell. They are anhydride bonds. Alpha is the closest P. It is an ester bond which yeilds less energy than gamma /beta P. |
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What is a high energy bond? |
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a bond with high group transfer potential. Pi would rather be transfered to a different "acceptor" molecule. It would rather be somewhere else |
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