
Concept explainers
Interpretation:
The following molecule is to be named.
Concept introduction:
To write the IUPAC name of an organic compound that contain a benzene ring, the steps to follow as:
1. Number the carbon atoms present in the benzene ring such that the substituents get the lowest locant number. The carbon
2. Specify the substituent position by number the carbon atom to which the substituent is bonded.
3. If there are more substituents in the compound, then they are named according to the alphabetical order.
4. Generally, the base name is benzene for benzene ring. The format to name the molecule that contains a benzene ring is as follows:

Want to see the full answer?
Check out a sample textbook solution
Chapter 21 Solutions
Introductory Chemistry: An Active Learning Approach
- 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
- Introductory Chemistry: An Active Learning Approa...ChemistryISBN:9781305079250Author:Mark S. Cracolice, Ed PetersPublisher:Cengage LearningLiving By Chemistry: First Edition TextbookChemistryISBN:9781559539418Author:Angelica StacyPublisher:MAC HIGHERChemistry: The Molecular ScienceChemistryISBN:9781285199047Author:John W. Moore, Conrad L. StanitskiPublisher:Cengage Learning
- Chemistry: Matter and ChangeChemistryISBN:9780078746376Author:Dinah Zike, Laurel Dingrando, Nicholas Hainen, Cheryl WistromPublisher:Glencoe/McGraw-Hill School Pub CoOrganic Chemistry: A Guided InquiryChemistryISBN:9780618974122Author:Andrei StraumanisPublisher:Cengage Learning



