Which of the following types of compounds is most likely to undergo racemization when treated with aqueous acid or base ( + or )?
5. Chirality
Optical Activity
- Multiple Choice55views
- Multiple Choice
Choose the best explanation for why a racemic mixture does not rotate plane-polarized light.
66views - Multiple Choice
Given the compound , determine whether it is optically active or optically inactive.
49views - Multiple ChoiceWhich alkane can exhibit optical activity due to the presence of a stereogenic (chiral) carbon atom?20views
- Textbook Question
a. Is (R)-lactic acid dextrorotatory or levorotatory?
b. Is (R)-sodium lactate dextrorotatory or levorotatory?
1229views - Textbook Question
Explain how R and S are related to (+) and (-).
1479views - Textbook Question
The reaction of (R)-1-iodo-2-methylbutane with hydroxide ion forms an alcohol without breaking any bonds to the asymmetric center. The alcohol rotates the plane of polarization of plane-polarized light counterclockwise. What is the configuration of (+)-2-methyl-1-butanol?
1100views - Textbook Question
Which of the following are optically active?
1666views - Textbook Question
Which stereoisomers are optically inactive?
1511views - Textbook Question
Make a model of each compound, draw it in its most symmetric conformation, and determine whether it is capable of showing optical activity.
a. 1-bromo-1-chloroethane
b. 1-bromo-2-chloroethane
1102views - Textbook Question
Based on the absolute configuration of (S)-butan-2-ol, what can you say about the direction it rotates plane-polarized light?
862views - Textbook Question
Naproxen is a commercially available anti-inflammatory sold under the name Aleve.
(b) Given that naproxen rotates plane-polarized light in the clockwise direction, should it be referred to as (d) or (l)?
(c) Is it (+) or (-)?
(d) What direction (d or l; + or −) would you expect the enantiomer of naproxen to rotate plane-polarized light?
964views - Textbook Question
When the following substituted biphenyl was synthesized, it was found to have a specific rotation [α] of -23° at 25°C . When the specific rotation was measured at 100°C the compound had a specific rotation of 0° . Upon cooling back to 25°C the specific rotation was measured again, resulting in [α] = 0°. Explain these results.
590views - Textbook Question
(R)-Limonene is a cyclic terpene responsible for the smell of oranges and other citrus fruits.
(a) Given that (R)-limonene rotates plane-polarized light in the clockwise direction, should it be referred to as (d) or (l)?
(b) Is it (+) or (-)?
(c) What direction (d or l; + or −) would you expect (S)-limonene to rotate plane-polarized light?
714views - Textbook Question
Which of the following diastereomers of hexane-2,5-diol is optically inactive? Why?
779views