(Print) Use this randomly generated list as your call list when playing the game. There is no need to say the BINGO column name. Place some kind of mark (like an X, a checkmark, a dot, tally mark, etc) on each cell as you announce it, to keep track. You can also cut out each item, place them in a bag and pull words from the bag.
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isomers that are not mirror images
diastereomers
product when oxidize an aldehyde
carboxylic acid
acid chloride, acid anhydride, and amide
carboxylic acid derivatives
contains 2 -OR groups on same carbon
acetal
disaccharide with 2 glucoses and alpha 1-4 linkage
maltose
aldehyde common name w/ 1 carbons
formaldehyde
galactose is known as a:
brain sugar
positive Tollen's test
silver mirror formation
reduction of sugar produces an:
alditol
carbon w/ 4 different groups
chiral
product when COOH reacts w/ water
carboxylate ion
carb with ketone and 5 carbons
ketopentose
hydrolysis of ester under basic conditions
saponification
carb with aldehyde and 6 carbons
aldohexose
product when ketone is reduced
secondary alcohol
contains -OH and -OR on same carbon
hemiacetal
common name for COOH w/ 1 carbon
formic acid
have a polar C-Z bond
acyl compounds
suffix used for naming ketones
-one
disaccharide with glucose + fructose
sucrose
abbreviation for a carboxylic acid
COOH
anomeric carbon points down
beta anomer
polyfunctional acid with hydroxyl group
hydroxy acids
disaccharide with 2 glucose + galactose
lactose
Benedict's Test
test for aldehydes
non-superimposable mirror images
enantiomers
aldehyde common name w/ 4 carbons
butyraldehyde
lactose is known as a:
milk sugar
polysaccharide with all glucose, alpha 1-4 bonds, and no branch points
amylose
polyfunctional acid with carbonyl group
keto acid
have a non-polar C-Z bond
carbonyl compounds
product when COOH reacts w/ an alcohol
ester
anomeric carbon points down
alpha anomer
heparin and hyaluronic acid are:
acidic polysaccharide
strong oxidation of sugar produces an:
aldaric acid
aldehyde common name w/ 3 carbons
propionaldehyde
polyfunctional acid with double bonds
unsaturated acid
starch and glycogen are:
storage polysaccharides
common name for COOH w/ 5 carbons
valeric acid
cellulose and chitin are:
structural polysaccharides
biologically relevant carbohydrates
D-enantiomer
suffix for acyl portion of an ester
-oate
common name for COOH w/ 2 carbons
acetic acid
polysaccharide with all glucose, alpha 1-4 bonds, and some alpha 1-6 branch points
amylopectin
how to ID the D-enantiomer for cyclic carbs
CH2OH points up
removes a CO2 from the molecule
decarboxylation
has -OH on left side of Fisher projection
L-enantiomer
suffix for COOH
-oic acid
aldehyde common name w/ 2 carbons
acetaldehyde
suffix used for naming aldehydes
-al
product when COOH reacts w/ a strong base
carboxylic acid salt
disaccharide with 2 glucoses and beta1-4 linkage
cellobiose
weak oxidation of sugar produces an:
aldonic acid
polysaccharide with all glucose, beta 1-4 bonds, and no branch points
cellulose
how to ID the L-enantiomer for cyclic carbs
CH2OH points down
sugar with free anomeric carbon (sucrose)
reducing sugar
product when oxidize a primary alcohol
aldehyde
COOH and CHO groups are:
always found at end of parent chain
