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3.0qt into mL


2. For an organic molecule to be chiral, it must have a chiral carbon, i.e., a carbon with four different substituents. Draw the structural formulas of the following molecules indicating which (if any) carbons are chiral:

a. Ethanol

b. Lactic Acid

c. Alanine

d. Chlorocyclohexane

e. 2-Bromochlorocyclohexane

f. meta-Dichlorobenzene

g. 2-Bromobutane

h. 3-ChloropentanE

i. 2-Bromo-3-chloropentane

j. 1-Chloro-2-bromo-3-heptanol



2,4-butanediol


For geometric stereoisomerism, include cis and

trans (Z and E) stereoisomers of unsaturated

fatty acids (e.g. oleic acid and elaidic acid).


Draw one example each of compounds fitting the
alkene, secondary amine and primary alcohol functional
descriptions below. There are many possible correct
answers for these.
a) A compound with molecular formula C6H11NO that includes
groups.
Conversion of octanal to 2-octyne
Synthesis of octanal from bromo-2-octene

Name the following compounds. Please include the stereochemical assignment (cis/trans, E/Z and R/S in the name where applicable. OH NH2 O O


Synthesis of octanal from bromo-2-propylpentane

What are the bond angles and lengths of pyruvic acid?

Angles and lengths for all bonds, please.