(a)
Interpretation:
From the given compounds from E to H, a compound containing a primary amine and a primary amide needs to be identified.
Concept Introduction:
Amine − is an organic N compounds formed by replacing one or more H atoms of
Amide- is an organic compound contains the group of

Answer to Problem 31P
Structure H.
Explanation of Solution
Amines are formed by replacing one or more hydrogen atoms of ammonia with alkyl groups.
Furthermore,
In the below structure, bond that is indicated in red color is the single
Hence, structure H is a compound that contains a
(b)
Interpretation:
From the given compounds from E to H, a compound containing a primary amine and a secondary amide needs to be identified.
Concept Introduction:
Amine − is an organic N compounds formed by replacing one or more H atoms of
Amide- is an organic compound contains the group of

Answer to Problem 31P
Structure F.
Explanation of Solution
Amines are formed by replacing one or more hydrogen atoms of ammonia with alkyl groups.
Furthermore,
In the below structure, bonds that are indicated in red color are the two
Hence, structure F is a compound that contains a
(c)
Interpretation:
From the given compounds from E to H, a compound containing a secondary amine and a tertiary amide needs to be identified.
Concept Introduction:
Amine − is an organic N compounds formed by replacing one or more H atoms of
Amide- is an organic compound contains the group of

Answer to Problem 31P
Structure E.
Explanation of Solution
Amines are formed by replacing one or more hydrogen atoms of ammonia with alkyl groups.
Furthermore,
In the below structure, bonds that are indicated in red color are the three
Hence, structure E is a compound that contains a
(d)
Interpretation:
From the given compounds from E to H, a compound containing a tertiary amine and a tertiary amide needs to be identified.
Concept Introduction:
Amine − is an organic N compounds formed by replacing one or more H atoms of
Amide- is an organic compound contains the group of

Answer to Problem 31P
Structure G.
Explanation of Solution
Amines are formed by replacing one or more hydrogen atoms of ammonia with alkyl groups.
Furthermore,
In the below structure, bonds that are indicated in red color are the three
Hence, structure G is a compound that contains a
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Chapter 18 Solutions
GENERAL,ORGANIC, & BIOLOGICAL CHEM-ACCES
- Polymers may be composed of thousands of monomers. draw two repeat units(dimer) of the polymer formed in this reaction. assume there are hydrogen atoms on the two ends of the dimer. ignore inorganic byproducts pleasearrow_forwardDraw the product of the reaction shown below. Use a dash or wedge bond to indicate stereochemistry of substituents on asymmetric centers, Ignore inorganic byproductsarrow_forwardDraw the product of this reaction please. Ignore inorganic byproductsarrow_forward
- One of the pi molecular orbitals of 1,3-butadiene (CH2=CHCH=CH2) is shown below. Please identify the number of nodal planes perpendicular to the bonding axisarrow_forwardDraw the monomers required to synthesize this condensation polymer please.arrow_forwardProvide the correct systematic name for the compound shown here. Please take into account the keyboard options belowarrow_forward
- curved arrows are used to illustrate the flow of electrons. using the provided starting and product structures, draw the curved electron-pushing arrows for the following reaction or mechanistic step(s)arrow_forwardIdentify the 'cartoon' drawing of the acceptor orbital in the first mechanistic step of an electrophilic addition reaction of butadiene with HBr. Pleasearrow_forwardH- H H H H H H Identify and select all structures below that represent a constitutional isomer(s) of the compound shown above. H- H H H A. H H H H-C CI H H D. H H H H H H C C -H H C C H H H H B. H CI H H- C C H H H H E. H CI H C.arrow_forward
- Why doesn't this carry on to form a ring by deprotonating the alpha carbon and the negatively-charged carbon attacking the C=O?arrow_forward6. A solution (0.0004 M) of Fe(S2CNEt2)3 (see the structural drawing below) in chloroform has absorption bands at: 350 nm (absorbance A = 2.34); 514 nm(absorbance A = 0.0532); Calculate the molar absorptivity values for these bands. Comment on their possible nature (charge transfer transitions or d-d S N- transitions?). (4 points)arrow_forwardWhat is the mechanism for this?arrow_forward
- Chemistry: The Molecular ScienceChemistryISBN:9781285199047Author:John W. Moore, Conrad L. StanitskiPublisher:Cengage Learning

