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