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

Author Question: Which of the following compounds are primary (1) amines? a. 1 and 2 b. 1 and 3 c. 1, 2 ... (Read 27 times)

maegan_martin

  • Hero Member
  • *****
  • Posts: 532
Which of the following compounds are primary (1) amines?
   
 
   
  a.
  1 and 2
  b.
  1 and 3
  c.
  1, 2 and 3
  d.
  1, 2, 3 and 4

Question 2

Instructions: Give the major organic product(s) of each of the following reaction or sequence of reactions. Show all relevant stereochemistry.
   
  Give the major product(s).
   
 

Question 3

Instructions: Give the major organic product(s) of each of the following reaction or sequence of reactions. Show all relevant stereochemistry.
   
  Give major product(s):
   
 

Question 4

Instructions: Give the major organic product(s) of each of the following reaction or sequence of reactions. Show all relevant stereochemistry.
   
   
 

Question 5

Instructions: Give the major organic product(s) of each of the following reaction or sequence of reactions. Show all relevant stereochemistry.
   
  Give major product(s):
   
 

Question 6

Instructions: Give the major organic product(s) of each of the following reaction or sequence of reactions. Show all relevant stereochemistry.
   
  Give major product(s):
   
 

Question 7

Rank the following compounds in order of increasing basicity. Label the least basic compound 1 and the most basic compound 4. Place the number corresponding to the compound's rank in the blank below the compound.
   
 

Question 8

In the following series of compounds, which is the most basic and the least basic? Explain your choices.
   
 

Question 9

Circle any of the following that would be classified as a heterocyclic amine.
   
 

Question 10

Instructions: Consider the reaction below to answer the following question(s).
   
  Methamphetamine can be synthesized by reacting phenyl-2-propanone with methylamine in the presence of H2/Ni.
   
 
  Refer to instructions. Although the yield of methamphetamine is good, some unreacted phenyl-2-propanone remains after the reaction is complete. Describe how methamphetamine can be separated from phenyl-2-propanone.

Question 11

Instructions: Consider the reaction below to answer the following question(s).
   
  Methamphetamine can be synthesized by reacting phenyl-2-propanone with methylamine in the presence of H2/Ni.
   
 
  Refer to instructions. The synthesis of methamphetamine by reaction of 2-phenyl-2 propanone with methylamine in the presence of H2/Ni is referred to as:
   
  a.
  reductive nitrogenation
  b.
  reactive nitrogenation
  c.
  reductive amination
  d.
  reactive amination

Question 12

Instructions: Consider the reaction below to answer the following question(s).
   
  Methamphetamine can be synthesized by reacting phenyl-2-propanone with methylamine in the presence of H2/Ni.
   
 
  Refer to instructions. Intermediate A is an example of:
  a.
  an imine
  b.
  an enamine
  c.
  an iminium ion
  d.
  an imide

Question 13

Instructions: Consider the reaction below to answer the following question(s).
   
  Methamphetamine can be synthesized by reacting phenyl-2-propanone with methylamine in the presence of H2/Ni.
   
 
  Refer to instructions. Identify the nucleophile in the initial reaction of phenyl-2-propanone to yield intermediate A and classify the type of reaction that produces the final product from A.

Question 14

Instructions: Based on the following structures, name the compound.
  Name:
   
 

Question 15

Instructions: Based on the following structures, name the compound.
  Name:
   
 

Question 16

Instructions: Based on the following structures, name the compound.
  Name:
   
 

Question 17

Instructions: Based on the following structures, name the compound.
  Name:
   
 

Question 18

Instructions: Draw structures corresponding to each of the IUPAC names given in the following question(s).
  Draw:
   
   N,N-dimethylcyclopentylamine

Question 19

Instructions: Draw structures corresponding to each of the IUPAC names given in the following question(s).
  Draw:
   
   hexane-1,6-diamine



Related Topics

Need homework help now?

Ask unlimited questions for free

Ask a Question
Marked as best answer by a Subject Expert

tdewitt

  • Sr. Member
  • ****
  • Posts: 318
Answer to Question 1

c

Answer to Question 2



Answer to Question 3



Answer to Question 4



Answer to Question 5



Answer to Question 6



Answer to Question 7



Answer to Question 8

ANS: CH3CH2CH2NH2

Strongest base because it is the only aliphatic amine.



Weakest based because it is an amide not an amine and is not considered basic.

Answer to Question 9



Answer to Question 10

Dissolve the reaction mixture containing the ketone and amine in ether and extract with aqueous HCl. The basic amine will dissolve in the aqueous layer as its hydrochloric salt. The neutral ketone will remain in the ether layer. Separate the two layers and neutralize the aqueous layer with NaOH. Extract the neutralized layer with ether. The purified amine will dissolve in the ether.

Answer to Question 11

c

Answer to Question 12

a

Answer to Question 13

ANS: The nucleophile is methylamine and the final (second) reaction is a reduction.

Answer to Question 14

ANS: 2,4-hexanediamine

Answer to Question 15

ANS: N-ethylaniline

Answer to Question 16

ANS: methyl-2-aminobutanoate

Answer to Question 17

ANS: p-methoxyaniline or 4-methoxyaniline

Answer to Question 18



Answer to Question 19

ANS: H2NCH2CH2 CH2CH2CH2CH2NH2




tdewitt

  • Sr. Member
  • ****
  • Posts: 318

 

Did you know?

Liver spots have nothing whatsoever to do with the liver. They are a type of freckles commonly seen in older adults who have been out in the sun without sufficient sunscreen.

Did you know?

In 1835 it was discovered that a disease of silkworms known as muscardine could be transferred from one silkworm to another, and was caused by a fungus.

Did you know?

Your skin wrinkles if you stay in the bathtub a long time because the outermost layer of skin (which consists of dead keratin) swells when it absorbs water. It is tightly attached to the skin below it, so it compensates for the increased area by wrinkling. This happens to the hands and feet because they have the thickest layer of dead keratin cells.

Did you know?

Though Candida and Aspergillus species are the most common fungal pathogens causing invasive fungal disease in the immunocompromised, infections due to previously uncommon hyaline and dematiaceous filamentous fungi are occurring more often today. Rare fungal infections, once accurately diagnosed, may require surgical debridement, immunotherapy, and newer antifungals used singly or in combination with older antifungals, on a case-by-case basis.

Did you know?

Oxytocin is recommended only for pregnancies that have a medical reason for inducing labor (such as eclampsia) and is not recommended for elective procedures or for making the birthing process more convenient.

For a complete list of videos, visit our video library