
Concept explainers
(a)
Interpretation: Primary, secondary and tertiary hydrogen in structure of ethane should be labeled.
Concept introduction: In accordance with IUPAC convention longest chain can be found from either direction provided it is longest and digits indicate the position of carbon or the position of branched alkyl chain in cases of branched hydrocarbons. All the side chains are named in alphabetical order.
The IUPAC system for nomenclature of straight hydrocarbon makes use of table given as follows:
Beside the IUPAC names there are certain common names. The common prefixes used include prefixes “iso-” and “neo-”.For example, isobutane is common name used popularly for
The carbon linked to one alkyl/carbon while other two
The carbon linked to two alkyl /carbons and one
The carbon linked to three alkyl groups/carbons and no
These are indicated below:
(b)
Interpretation: Primary, secondary and tertiary hydrogen in structure of pentane should be labeled.
Concept introduction: In accordance with IUPAC convention longest chain can be found from either direction provided it is longest and digits indicate the position of carbon or the position of branched alkyl chain in cases of branched hydrocarbons. All the side chains are named in alphabetical order.
The IUPAC system for nomenclature of straight hydrocarbon makes use of table given as follows:
Beside the IUPAC names there are certain common names. The common prefixes used include prefixes “iso-” and “neo-”.For example, isobutane is common name used popularly for
The carbon linked to one alkyl/carbon while other two
The carbon linked to two alkyl /carbons and one
The carbon linked to three alkyl groups/carbons and no
These are indicated below:
(c)
Interpretation: Primary, secondary and tertiary hydrogen in structure of
Concept introduction: In accordance with IUPAC convention longest chain can be found from either direction provided it is longest and digits indicate the position of carbon or the position of branched alkyl chain in cases of branched hydrocarbons. All the side chains are named in alphabetical order.
The IUPAC system for nomenclature of straight hydrocarbon makes use of table given as follows:
Beside the IUPAC names there are certain common names. The common prefixes used include prefixes “iso-” and “neo-”. For example, isobutane is common name used popularly for
The carbon linked to one alkyl/carbon while other two
The carbon linked to two alkyl /carbons and one
The carbon linked to three alkyl groups/carbons and no
These are indicated below:
(d)
Interpretation: Primary, secondary and tertiary carbons in structure of
Concept introduction: In accordance with IUPAC convention longest chain can be found from either direction provided it is longest and digits indicate the position of carbon or the position of branched alkyl chain in cases of branched hydrocarbons. All the side chains are named in alphabetical order.
The IUPAC system for nomenclature of straight hydrocarbon makes use of table given as follows:
Beside the IUPAC names there are certain common names. The common prefixes used include prefixes “iso-” and “neo-”. For example, isobutane is common name used popularly for
The carbon linked to one alkyl/carbon while other two
The carbon linked to two alkyl /carbons and one
The carbon linked to three alkyl groups/carbons and no

Want to see the full answer?
Check out a sample textbook solution
Chapter 2 Solutions
EBK ORGANIC CHEMISTRY
- 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
- ChemistryChemistryISBN:9781305957404Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCostePublisher:Cengage LearningChemistryChemistryISBN:9781259911156Author:Raymond Chang Dr., Jason Overby ProfessorPublisher:McGraw-Hill EducationPrinciples of Instrumental AnalysisChemistryISBN:9781305577213Author:Douglas A. Skoog, F. James Holler, Stanley R. CrouchPublisher:Cengage Learning
- Organic ChemistryChemistryISBN:9780078021558Author:Janice Gorzynski Smith Dr.Publisher:McGraw-Hill EducationChemistry: Principles and ReactionsChemistryISBN:9781305079373Author:William L. Masterton, Cecile N. HurleyPublisher:Cengage LearningElementary Principles of Chemical Processes, Bind...ChemistryISBN:9781118431221Author:Richard M. Felder, Ronald W. Rousseau, Lisa G. BullardPublisher:WILEY





