
EBK ORGANIC CHEMISTRY AS A SECOND LANGU
4th Edition
ISBN: 8220102737037
Author: Klein
Publisher: YUZU
expand_more
expand_more
format_list_bulleted
Question
Chapter 1.2, Problem 1.6P
Interpretation Introduction
Interpretation:
A systematic name for the given compound has to be provided.
Concept Introduction:
Nomenclature of
- The parent is benzene ring.
Functional groups attached to it other than hydrogens are called substituents. The name of substituent must be placed before the name of the compound as a prefix in any substituted hydrocarbon.Ex.
- The numerical prefixes such as di, tri, and tetra must be included in the nomenclature if more than one similar substituents are attached to the benzene ring.
Ex.
- If different substituent groups are attached to the benzene ring, the no. one position is determined by the parent. So the first step is to choose a suitable parent. Then the locants are assigned in a manner that gives the lower possible number to the next substituent.
Ex.
- For disubstituted benzenes, prefixes such as ortho, meta and para should be used.
Ex.
Expert Solution & Answer

Want to see the full answer?
Check out a sample textbook solution
Students have asked these similar questions
For the reaction A (g) → 3 B (g), Kp = 0.379 at 298 K. What is the value of ∆G for this reaction at 298 K when the partial pressures of A and B are 5.70 atm and 0.250 atm?
14. Calculate the concentrations of Ag+, Ag(S2O3), and Ag(S2O3)23- in a solution prepared by mixing
150.0 mL of 1.00×10-3 M AgNO3 with 200.0 mL of 5.00 M Na2S2O3
Ag+ + S20
Ag(S203)¯
K₁ = 7.4 × 108
Ag(S203)¯ + S20¯ = Ag(S203)
K₂ = 3.9 x 104
ΗΝ,
cyclohexanone
pH 4-5
Draw Enamine
I
I
CH3CH2Br
THF, reflux
H3O+
I
Drawing
Draw Iminium Ion
Chapter 1 Solutions
EBK ORGANIC CHEMISTRY AS A SECOND LANGU
Ch. 1.2 - Prob. 1.2PCh. 1.2 - Prob. 1.3PCh. 1.2 - Prob. 1.4PCh. 1.2 - Prob. 1.5PCh. 1.2 - Prob. 1.6PCh. 1.3 - Characterize each of the following structures as...Ch. 1.3 - Characterize each of the following structures as...Ch. 1.3 - Characterize each of the following structures as...Ch. 1.3 - Characterize each of the following structures as...Ch. 1.3 - Characterize each of the following structures as...
Knowledge Booster
Similar questions
- :0: :0: Select to Add Arrows :0: (CH3)2NH :0: ■ Select to Add Arrows :0: :0: (CH3)2NH ■ Select to Add Arrowsarrow_forwardDraw the product of the following H action sequence. Ignore any inorganic byproducts formed. 1. (CH3CH2)2CuLi, THF 2. CH3Br Q Atoms, Bonds and Rings H Charges ㅁarrow_forwardPlease help me with this the problem is so confusingarrow_forward
- 14 Question (1 point) Disiamylborane adds to a triple bond to give an alkenylborane. Upon oxidation with OH, H2O2, the alkenylborane will form an enol that tautomerizes to an aldehyde. In the first box below, draw the mechanism arrows for the reaction of disiamylborane with the alkyne, and in the last box draw the structure of the aldehyde. 4th attempt Feedback i > 3rd attempt OH, H2O2 i See Periodic Table See Hintarrow_forwardanswer with mechanisms and steps. handwritten please!arrow_forwardHello I need some help with Smartwork. For drawing structure B, I know the correct answer is CH₃B₂, but when I try to type it in, it keeps giving me CH₄BH₃ instead. Do you know how I should write it properly? Should I use a bond or something else?arrow_forward
arrow_back_ios
SEE MORE QUESTIONS
arrow_forward_ios
Recommended textbooks for you
- Chemistry for Today: General, Organic, and Bioche...ChemistryISBN:9781305960060Author:Spencer L. Seager, Michael R. Slabaugh, Maren S. HansenPublisher:Cengage LearningChemistry: Matter and ChangeChemistryISBN:9780078746376Author:Dinah Zike, Laurel Dingrando, Nicholas Hainen, Cheryl WistromPublisher:Glencoe/McGraw-Hill School Pub CoIntroductory Chemistry: A FoundationChemistryISBN:9781285199030Author:Steven S. Zumdahl, Donald J. DeCostePublisher:Cengage Learning
- Introductory Chemistry: An Active Learning Approa...ChemistryISBN:9781305079250Author:Mark S. Cracolice, Ed PetersPublisher:Cengage LearningChemistry: The Molecular ScienceChemistryISBN:9781285199047Author:John W. Moore, Conrad L. StanitskiPublisher:Cengage Learning

Chemistry for Today: General, Organic, and Bioche...
Chemistry
ISBN:9781305960060
Author:Spencer L. Seager, Michael R. Slabaugh, Maren S. Hansen
Publisher:Cengage Learning
Chemistry: Matter and Change
Chemistry
ISBN:9780078746376
Author:Dinah Zike, Laurel Dingrando, Nicholas Hainen, Cheryl Wistrom
Publisher:Glencoe/McGraw-Hill School Pub Co

Introductory Chemistry: A Foundation
Chemistry
ISBN:9781285199030
Author:Steven S. Zumdahl, Donald J. DeCoste
Publisher:Cengage Learning


Introductory Chemistry: An Active Learning Approa...
Chemistry
ISBN:9781305079250
Author:Mark S. Cracolice, Ed Peters
Publisher:Cengage Learning

Chemistry: The Molecular Science
Chemistry
ISBN:9781285199047
Author:John W. Moore, Conrad L. Stanitski
Publisher:Cengage Learning