Open chain and ring structures ofmonosaccharides1
Open%chain%and%ring%structures%of% monosaccharides 1%
1. Aldoses and ketoses: openchain structuresEmpirical formula CH,O (hydrated carbon)Contain an oxygen atom attached to each carbonHighlyfunctionalizedCH2OHCHOLinear carbon chainC=O(CHOH)nAldehyde at C-1(CHOH)nCH2OHVarious secondary alcoholCH2OHaldosesAprimaryalcohol at theendketosesprimary alcohols at both endsKetone withinthechain
1.%Aldoses%and%ketoses:%open% chain%structures Empirical%formula%CH2O%(hydrated%carbon)% Contain%an%oxygen%atom%aBached%to%each%carbon% Highly%funcConalized% Linear%carbon%chain% Aldehyde%at%CF1% Various%secondary%alcohol% A%primary%alcohol%at%the%end% primary%alcohols%at%both%ends% Ketone%within%the%chain% 2%
CHOCHOCHOCHO(CHOH),(CHOH),CHOH(CHOH)CH20OHCH2OHCH2OHCH20HglyceraldehydetetrosepentosehexoseCHOCHO1111OHHHHOICH2OHCH2OH三CHOCHOC-OHHO-CCH2OHCH2OHD- or R-L- or S-3
3%
1.1 Erythrose and therosediastereomersenantiomersn CHOH groups, 2n stereoisomersconfigurationconformationeclipsedstaggeredZigzag drawingFischerprojection
1.1#Erythrose#and#therose 4% n%CHOH%groups,%2n%stereoisomers%
Newman projections:0=000HHH0=60°HHHHHHHHHHHHHHHSawhorse structures:HHHHHHHHHHHHHH-HHHHeclipsed,=00staggered,0=60skew, = anything else5
5%