Chapter 3: Q66P (page 138)
Draw a picture of the hydrogen bonding in methanol.
Chapter 3: Q66P (page 138)
Draw a picture of the hydrogen bonding in methanol.
All the tools & learning materials you need for study success - in one app.
Get started for freea. Which of the following compounds forms hydrogen bonds between its molecules?
1. CH3CH2OCH2CH2OH 3. CH3CH2CH2CH2Br 5. CH3CH2CH2COOH
2. CH3CH2N(CH3)2 4. CH3CH2CH2NHCH3 6. CH3CH2CH2CH2F
b. Which of the preceding compounds forms hydrogen bonds with a solvent such as ethanol?
Draw the structures and provide systematic names for parts a, b, and c by substituting a chlorine for a hydrogen of methylcyclohexane:
a. A primary alkyl halide
b. A tertiary alkyl halide
c. Three secondary alkyl halides
What is each compoundโs systematic name?
Draw all the isomers that have molecular formula C5H12Br. (Hint: There are eight.)
a. Give the systematic name for each of the isomers.
b. Give a common name for each isomer that has a common name.
c. How many of the isomers are primary alkyl halides?
d. How many of the isomers are secondary alkyl halides?
e. How many of the isomers are tertiary alkyl halides?
a. Draw a potential energy diagram for rotation about the C-C bond of 1,2-dichloroethane through 360degree, starting with the least stable conformer. The anti-conformer is 1.2 kcal/mol more stable than a gauche conformer. A gauche conformer has two energy barriers, 5.2 kcal/mol and 9.3 kcal/mol.
b. Draw the conformer that is present in greatest concentration.
c. How much more stable is the most stable staggered conformer than the most stable eclipsed conformer?
d. How much more stable is the most stable staggered conformer than the least stable eclipsed conformer?
What do you think about this solution?
We value your feedback to improve our textbook solutions.