Reactions I
Chirality Definitions
Optical Isomers I
True or False?
100

What is the result of oxidizing a ketone?

No reaction

100

What is a chiral center/compound?

a chiral compound must have at least 1 chiral center. 

chiral centers are atoms with 4 bonds in which each bond is to a different atom or functional group.

100

What does a D-isomer refer to?

Isomer that spins towards the dextrorotatory (right, clockwise) direction.

100

T/F: diastereomers can show optical isomerism?

False; optical isomers must be mirror images of each other

200

If you add an alcohol to a carboxylic acid, the product is an...

ester

200

What is an enantiomer?

A molecule can be drawn that in two ways in which the two forms are mirror images of each other, but cannot be superimposed on each other (if you put one on top of the other, it wouldn't match).

200

What does a L-isomer refer to?

Isomer that spins towards the dextrorotatory (right, clockwise) direction.

200

T/F: If one form of an enantiomer has two chiral centers with (R, R) configuration, the other enantiomer has (S, S) configuration.

True

300

If you add a carboxylic acid to a primary or secondary amine, you get a(n)...

amide

300

What is a diastereomer?

A compound that shares a molecular formula with another distinct compound, but the compounds are NOT mirror images of each other.

300

What does an (S)-isomer refer to?

the configuration of the atoms surrounding the chiral center from least to greatest organized in the left (counterclockwise) direction.

300
T/F: cis-trans isomerism is a type of geometric isomerism, which makes them enantiomers.

False; they are diastereomers

400

The Tollen's test is a test for what?

Aldehyde (or alpha-hydroxy ketone)

400

What is a meso compound?

A compound with an internal plane of symmetry that makes them optically inactive.

400

What does and (_R)-isomer refer to?

the configuration of the atoms surrounding the chiral center from least to greatest organized in the right (clockwise) direction.

400

T/F: For a Fischer projection, as long as you identify the priority of the compounds and determine the direction (R or S), that is automatically the correct answer.

False, you need to consider if the lowest priority group is in the front or the back of the projection. If it is in the front, the configuration is the opposite of the one you determine by looking at the projection.

500

The bromine test is a test for what? What gets colored by the bromine?

unsaturation (double bonds, triple bonds); saturated (single) bond compounds

500

What type of isomer are cis/trans isomers?

diastereomers

500

Which Letter System, D & L, or R & S, refers SOLEY to the experimental rotation of compounds when polarized by light?

D and L

500

T/F: A racemate is a mixture 50:50 of two enantiomers.

True

M
e
n
u