Chapter 4: Q11P (page 150)
Name each of the following:
Short Answer
The names of the given skeletal structures are:
a) (E)-2-heptene
b) (Z)-3,4-dimethyl-2-pentene
c) (Z)-1-chloro-3-ethyl-4-methyl-3-hexene
Chapter 4: Q11P (page 150)
Name each of the following:
The names of the given skeletal structures are:
a) (E)-2-heptene
b) (Z)-3,4-dimethyl-2-pentene
c) (Z)-1-chloro-3-ethyl-4-methyl-3-hexene
All the tools & learning materials you need for study success - in one app.
Get started for freeNaproxen, a nonsteroidal anti-inflammatory drug that is the active ingredient in Aleve (p. 115), has a specific rotation of +66. One commercial preparation result in a mixture with a 97% enantiomeric excess.
a. Does naproxen have the R or the S configuration?
b. What percent of each enantiomer is obtained from the commercial preparation?
The observed rotation of 2.0 g of a compound in 50 mL of solution in a polarimeter tube 20 cm long is +138°. What is the specific rotation of the compound?
Question:A compound has a specific rotation of -39.0. A solution of the compound (0.187 g/100 mL) has an observed rotation of -6.52° when placed in a polarimetertube 10 cm long. What is the percent of each enantiomer in the solution?
Draw a perspective formula for each of the following:
a. (S)-2-chlorobutane
b. (R)-1,2-dibromobutane
Assign relative priorities to each set of substituents:
a. -Br -I -OH -CH3
b. -CH2CH2OH -OH -CH2Cl -CH=CH2
What do you think about this solution?
We value your feedback to improve our textbook solutions.