This topic contains a solution. Click here to go to the answer

Author Question: Diethyl ether (CH3CH2OCH2CH3) and 1-butanol (CH3CH2CH2CH2OH) have similar solubility in water, but ... (Read 36 times)

ts19998

  • Hero Member
  • *****
  • Posts: 531

Diethyl ether (CH3CH2OCH2CH3) and 1-butanol (CH3CH2CH2CH2OH) have similar solubility in water,
  but 1-butanol has a much higher boiling point (118) than diethyl ether (35). Explain.



Question 2

Draw shorthand representations of each:
 

Question 3

Give the functional group of each molecule.
 

Question 4

Draw the four structural isomers with the formula C3H6C12

Question 5

Draw a reasonable structure for C6H8NO2Br.
 

Question 6

Draw five possible structural isomers for C4H7C1. (Do not show identical structures.)

Question 7

Which structure does not contain the functional group indicated?
 



Related Topics

Need homework help now?

Ask unlimited questions for free

Ask a Question
Marked as best answer by a Subject Expert

sierramartinez

  • Sr. Member
  • ****
  • Posts: 313
Answer to Question 1

Both diethyl ether and 1-butanol form hydrogen bonds with water (which furnishes the OH). 1-
Butanol can hydrogen bond with other 1-butanol molecules, but diethyl ether cannot hydrogen bond with
other diethyl ether molecules.



Answer to Question 2



Answer to Question 3

a. alcohol
b. carboxylic acid
c. ketone
d. aldehyde
e. amide
f. ester



Answer to Question 4



Answer to Question 5



Answer to Question 6



Answer to Question 7

c

Answer to Question 8

c

Answer to Question 9

b

Answer to Question 10

a





 

Did you know?

The average office desk has 400 times more bacteria on it than a toilet.

Did you know?

In women, pharmacodynamic differences include increased sensitivity to (and increased effectiveness of) beta-blockers, opioids, selective serotonin reuptake inhibitors, and typical antipsychotics.

Did you know?

The most destructive flu epidemic of all times in recorded history occurred in 1918, with approximately 20 million deaths worldwide.

Did you know?

The use of salicylates dates back 2,500 years to Hippocrates’s recommendation of willow bark (from which a salicylate is derived) as an aid to the pains of childbirth. However, overdosage of salicylates can harm body fluids, electrolytes, the CNS, the GI tract, the ears, the lungs, the blood, the liver, and the kidneys and cause coma or death.

Did you know?

All adverse reactions are commonly charted in red ink in the patient's record and usually are noted on the front of the chart. Failure to follow correct documentation procedures may result in malpractice lawsuits.

For a complete list of videos, visit our video library