a) N, N-Dimethylaniline
Interpretation:
The structure corresponding to the systematic name N, N-Dimethylaniline.
Answer to Problem 48AP
The IUPAC names given for the
Explanation of Solution
The longest carbon chain containing the double bond to be chosen. Based on the name of the parent compound – the
The IUPAC names given for the amines have the following structures.
b) (Cyclohexylmethyl) amine.
Interpretation:
The structure corresponding to the systematic name (Cyclohexylmethyl) amine.
Answer to Problem 48AP
The IUPAC names given for the amines have the following structures.
Explanation of Solution
The longest carbon chain containing the double bond to be chosen. Based on the name of the parent compound – the alkene name ends with the suffix –ene. The chain is to be numbered from the end that gives the lowest number to the carbon in double bond. Substituents are to be numbered according to their positions in the chain and listed alphabetically. The position of the double bond is indicated by giving the number of the first alkene carbon before the name of the parent name. If more than one double bond is present, their positions are indicated with the suffixes -diene, -triene and so on. The isomer that has similar groups on each carbon on the same side of the double bond is called as the cis isomer. The isomer that has similar groups on each carbon on the opposite side of the double bond is called as thetrans isomer.
The IUPAC names given for the amines have the following structures.
c) N-Methylcyclohexylamine
Interpretation:
The structure corresponding to the systematic name N-Methylcyclohexylamine.
Answer:
The IUPAC names given for the amines have the following structures.
Explanation:
The longest carbon chain containing the double bond to be chosen. Based on the name of the parent compound – the alkene name ends with the suffix –ene. The chain is to be numbered from the end that gives the lowest number to the carbon in double bond. Substituents are to be numbered according to their positions in the chain and listed alphabetically. The position of the double bond is indicated by giving the number of the first alkene carbon before the name of the parent name. If more than one double bond is present, their positions are indicated with the suffixes -diene, -triene and so on. The isomer that has similar groups on each carbon on the same side of the double bond is called as the cis isomer. The isomer that has similar groups on each carbon on the opposite side of the double bond is called as thetrans isomer.
Conclusion:
The IUPAC names given for the amines have the following structures.
Answer to Problem 48AP
The IUPAC names given for the amines have the following structures.
Explanation of Solution
The longest carbon chain containing the double bond to be chosen. Based on the name of the parent compound – the alkene name ends with the suffix –ene. The chain is to be numbered from the end that gives the lowest number to the carbon in double bond. Substituents are to be numbered according to their positions in the chain and listed alphabetically. The position of the double bond is indicated by giving the number of the first alkene carbon before the name of the parent name. If more than one double bond is present, their positions are indicated with the suffixes -diene, -triene and so on. The isomer that has similar groups on each carbon on the same side of the double bond is called as the cis isomer. The isomer that has similar groups on each carbon on the opposite side of the double bond is called as thetrans isomer.
The IUPAC names given for the amines have the following structures.
d) (2-Methylcyclohexyl) amine.
Interpretation:
The structure corresponding to the systematic name (2-Methylcyclohexyl) amine.
Answer to Problem 48AP
The IUPAC names given for the amines have the following structures.
Explanation of Solution
The longest carbon chain containing the double bond to be chosen. Based on the name of the parent compound – the alkene name ends with the suffix –ene. The chain is to be numbered from the end that gives the lowest number to the carbon in double bond. Substituents are to be numbered according to their positions in the chain and listed alphabetically. The position of the double bond is indicated by giving the number of the first alkene carbon before the name of the parent name. If more than one double bond is present, their positions are indicated with the suffixes -diene, -triene and so on. The isomer that has similar groups on each carbon on the same side of the double bond is called as the cis isomer. The isomer that has similar groups on each carbon on the opposite side of the double bond is called as thetrans isomer.
The IUPAC names given for the amines have the following structures.
e) 3-(N, N-Dimethylamino)propanoic acid.
Interpretation:
The structure corresponding to the systematic name 3-(N, N-Dimethylamino)propanoic acid.
Answer to Problem 48AP
The IUPAC names given for the amines have the following structures.
Explanation of Solution
The longest carbon chain containing the double bond to be chosen. Based on the name of the parent compound – the alkene name ends with the suffix –ene. The chain is to be numbered from the end that gives the lowest number to the carbon in double bond. Substituents are to be numbered according to their positions in the chain and listed alphabetically. The position of the double bond is indicated by giving the number of the first alkene carbon before the name of the parent name. If more than one double bond is present, their positions are indicated with the suffixes -diene, -triene and so on. The isomer that has similar groups on each carbon on the same side of the double bond is called as the cis isomer. The isomer that has similar groups on each carbon on the opposite side of the double bond is called as thetrans isomer.
The IUPAC names given for the amines have the following structures.
Want to see more full solutions like this?
Chapter 24 Solutions
Study Guide with Student Solutions Manual for McMurry's Organic Chemistry, 9th
- N Classify each of the following molecules as aromatic, antiaromatic, or nonaromatic. NH O aromatic O antiaromatic O nonaromatic O aromatic O antiaromatic O nonaromatic O aromatic O antiaromatic O nonaromatic Garrow_forwardThe conjugate base of alkanes is called alkides. Correct?.arrow_forwardName these organic compounds: structure Br name CH3 CH3 ☐ ☐arrow_forward
- HH H-C H -C-H HH Draw the Skeletal Structures & H Name the molecules HH H H H H-C-C-C-C-C-C-H HHH HHH H H HHHHHHH H-C-C-C-C-C-C-C-C-C-H HHHHH H H H Harrow_forwarddont provide AI solution .... otherwise i will give you dislikearrow_forwardName these organic compounds: structure name CH3 CH3 ☐ F F CH3 ☐ O Explanation Check 2025 McGraw Hill LLC. All Rights Reserved. Terms ofarrow_forward
- Classify each of the following molecules as aromatic, antiaromatic, or nonaromatic. ZI NH Explanation Check O aromatic O antiaromatic O nonaromatic O aromatic O antiaromatic H O nonaromatic O aromatic O antiaromatic O nonaromatic ×arrow_forwardPart I. Draw the stepwise reaction mechanism of each product (a, b, c, d, e, f) HO HO OH НОН,С HO OH Sucrose HO CH₂OH H N N HO -H H -OH KMnO4, Heat H OH CH₂OH (d) Phenyl Osatriazole OH НОН,С HO HO + Glacial HOAC HO- HO CH₂OH OH HO Fructose (a) Glucose OH (b) H₂N HN (c) CuSO4-5H2O, ethanol H N N N HO ·H H OH H OH N CH₂OH OH (f) Phenyl Osazone H (e) Carboxy phenyl osatriazole Figure 2.1. Reaction Scheme for the Total Synthesis of Fine Chemicalsarrow_forwardWhich molecule is the most stable? Please explain.arrow_forward
Chemistry for Today: General, Organic, and Bioche...ChemistryISBN:9781305960060Author:Spencer L. Seager, Michael R. Slabaugh, Maren S. HansenPublisher:Cengage Learning