ochem 2 test 4 Flashcards
(40 cards)
carbohydrate
an organic compound containing only H & O atoms in the ratio of 2 H to 1 O
monosaccharides
carbs that cant be hydrolyzed to simpler compounds; also called simple sugars
oligosaccharides
carbs containing only a few (2-10) linked monosaccharides
disaccharides
carbs containing 2 linked monosaccharides
polysaccharides
carbs containing many linked monosaccharides
aldose
monosaccharides containing an aldehyde function in its non-cyclic forn
ketose
a monosaccharide containing a ketone function in its non-cyclic form
triose
a monosaccharide containg 3 C’s, can be either aldose or ketose
tetrose, pentose, hexose
monosaccharide with 4, 5, 6 C’s respecitively
Fischer projection
2-D structural projection of a molecule giving information about its stereochemistry
aldotetrose
an aldose with 4 C’s
ketodetrose
a ketose 4 C’s
aldopentose, aldohexose
and aldose with 5 or 6 C’s
ketopentose, ketohexose
a ketose with
Fischer nomenclature
designation of a compound as D or L depending on whether the s.c. farthest from the carbonyl carbon has OH on the right (D) or on the left (L) in the F.P.
Tollen’s regents
Ag+ compexed with NH3 in “tollen’s test”- makes silver mirror
Fehling reagent
Cu 2+ complexed with tartrate ion in Fehling’s test- turns red
Benedicts reagent
Cu 2+ complexed with citrate ion in Benedicts test- turns red
reducing sugars
monosaccharides which reduce the active metal ion in tollens Fehlings, or benedicts reagents
polyols
polyhydroxyalcohols
alditols
polyols derived from reduction of aldoses
hemiacetal
a compound containing an alcohol and an ether function bonded to the same carbon
acetal
a compound containing 2 ether functions
furanose ring structure
the 5 member ring with 1 O as ring member formed in cyclic hemiacetal formation