
(a)
Interpretation:
The structure of diethylamine is to be drawn. The amine is to be identified as primary, secondary, or tertiary.
Concept introduction:
Trivial names of several
Depending on whether the number of alkyl groups attached to the nitrogen is one, two, or three, the amine is classified as primary, secondary, or tertiary amine.
(b)
Interpretation:
The structure of diethylpropylamine is to be drawn. The amine is to be identified as primary, secondary, or tertiary.
Concept introduction:
Trivial names of several amines are still in common use. The names of the trivial names of alkyl groups, attached to nitrogen in the amine, are written first, followed by the suffix amine.
Depending on whether the number of alkyl groups attached to the nitrogen is one, two, or three, the amine is classified as primary, secondary, or tertiary amine.
(c)
Interpretation:
The structure of allylmethylamine is to be drawn. The amine is to be identified as primary, secondary, or tertiary.
Concept introduction:
Trivial names of several amines are still in common use. The names of the trivial names of alkyl groups, attached to the nitrogen in the amine, are written first, followed by the suffix amine.
Depending on whether the number of alkyl groups attached to the nitrogen is one, two, or three, the amine is classified as primary, secondary, or tertiary amine.
(d)
Interpretation:
The structure of cyclopentylamine is to be drawn. The amine is to be identified as primary, secondary, or tertiary.
Concept introduction:
Trivial names of several amines are still in common use. The names of the trivial names of alkyl groups attached to the nitrogen in amine are written first, followed by the suffix amine.
Depending on whether the number of alkyl groups attached to the nitrogen is one, two, or three, the amine is classified as primary, secondary or tertiary amine.
(e)
Interpretation:
The structure of dibenzylamine is to be drawn. The alcohol is to be identified as primary, secondary, or tertiary.
Concept introduction:
Trivial names of several amines are still in common use. The names of the trivial names of alkyl groups attached to the nitrogen in the amine are written first, followed by the suffix amine.
Depending on whether the number of alkyl groups attached to the nitrogen is one, two or three, the amine is classified as primary, secondary or tertiary amine.

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Chapter E Solutions
EBK ORGANIC CHEMISTRY: PRINCIPLES AND M
- For each of the substituted benzene molecules below, determine the inductive and resonance effects the substituent will have on the benzene ring, as well as the overall electron-density of the ring compared to unsubstituted benzene. Molecule Inductive Effects O donating O withdrawing O no inductive effects Resonance Effects Overall Electron-Density ○ donating ○ withdrawing O no resonance effects O electron-rich O electron-deficient O similar to benzene Cl O donating O withdrawing ○ donating ○ withdrawing O no inductive effects O no resonance effects O Explanation Check O electron-rich O electron-deficient similar to benzene X © 2025 McGraw Hill LLC. All Rights Reserved. Terms of Use | Privacy Center | Accessarrow_forwardIdentifying electron-donating and For each of the substituted benzene molecules below, determine the inductive and resonance effects the substituent will have on the benzene ring, as well as the overall electron-density of the ring compared to unsubstituted benzene. Molecule Inductive Effects NH2 ○ donating NO2 Explanation Check withdrawing no inductive effects Resonance Effects Overall Electron-Density ○ donating O withdrawing O no resonance effects O donating O withdrawing O donating withdrawing O no inductive effects Ono resonance effects O electron-rich electron-deficient O similar to benzene O electron-rich O electron-deficient O similar to benzene olo 18 Ar 2025 McGraw Hill LLC. All Rights Reserved. Terms of Use | Privacy Center | Accessibilityarrow_forwardRank each of the following substituted benzene molecules in order of which will react fastest (1) to slowest (4) by electrophilic aromatic substitution. Explanation Check Х (Choose one) OH (Choose one) OCH3 (Choose one) OH (Choose one) © 2025 McGraw Hill LLC. All Rights Reserved. Terms of Use | Privacy Centerarrow_forward
- Assign R or S to all the chiral centers in each compound drawn below porat bg 9 Br Brarrow_forwarddescrive the energy levels of an atom and howan electron moces between themarrow_forwardRank each set of substituents using the Cahn-Ingold-Perlog sequence rules (priority) by numbering the highest priority substituent 1.arrow_forward
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