
(a)
Interpretation:The product formed in indicated reaction should be formulated and whether it is chiral and shows any optical activity or not should be determined.
Concept introduction: The carbonyl bond is polar with partial positive charge on carbon and partial negative charge on oxygen as illustrated below.
Thus it can undergo hydride addition at carbon and proton addition at oxygen. Certain reagents that are useful for such hydride addition at carbonyl carbon include
Optical activity refers to ability to rotate the plane polarized light. For example, if the light is passed through a substance and the light that emerges has radiations are confined to one plane only the substance is said to be optically active.
The earliest criteria for optical activity were presence of a chiral center. The chiral refer to species attached to four different substituents. Chiral center leads to existence of organic compounds as two enantiomeric forms. However chiral center alone is not sufficient condition for determination of optical activity.
The criteria to identify the optical activity are to look for absence of any symmetry element. The symmetry elements make any molecule optically inactive.
(b)
Interpretation: The product formed in indicated reaction should be formulated and whether it is chiral and shows any optical activity or not should be determined.
Concept introduction: The carbonyl bond is polar with partial positive charge on carbon and partial negative charge on oxygen as illustrated below.
Thus it can undergo hydride addition at carbon and proton addition at oxygen. Certain reagents that are useful for such hydride addition at carbonyl carbon include
Optical activity refers to ability to rotate the plane polarized light. For example, if the light is passed through a substance and the light that emerges has radiations are confined to one plane only the substance is said to be optically active.
The earliest criteria for optical activity were presence of a chiral center. The chiral refer to species attached to four different substituents. Chiral center leads to exists of organic compounds as two enantiomeric forms. However chiral center alone is not sufficient condition for determination of optical activity.
The criteria to identify the optical activity are to look for absence of any symmetry element. The symmetry elements make any molecule optically inactive.
(c)
Interpretation: The product formed in indicated reaction should be formulated and whether it is chiral and shows any optical activity or not should be determined.
Concept introduction:The carbonyl bond is polar with partial positive charge on carbon and partial negative charge on oxygen as illustrated below.
Thus it can undergo hydride addition at carbon and proton addition at oxygen. Certain reagents that are useful for such hydride addition at carbonyl carbon include
Optical activity refers to ability to rotate the plane polarized light. For example, if the light is passed through a substance and the light that emerges has radiations are confined to one plane only the substance is said to be optically active.
The earliest criteria for optical activity were presence of a chiral center. The chiral refer to species attached to four different substituents. Chiral center leads to exists of organic compounds as two enantiomeric forms. However chiral center alone is not sufficient condition for determination of optical activity.
The criteria to identify the optical activity are to look for absence of any symmetry element. The symmetry elements make any molecule optically inactive.
(d)
Interpretation: The product formed in indicated reaction should be formulated and whether it is chiral and shows any optical activity or not should be determined.
Concept introduction:The carbonyl bond is polar with partial positive charge on carbon and partial negative charge on oxygen as illustrated below.
Thus it can undergo hydride addition at carbon and proton addition at oxygen. Certain reagents that are useful for such hydride addition at carbonyl carbon include
Optical activity refers to ability to rotate the plane polarized light. For example, if the light is passed through a substance and the light that emerges has radiations are confined to one plane only the substance is said to be optically active.
The earliest criteria for optical activity were presence of a chiral center. The chiral refer to species attached to four different substituents. Chiral center leads to exists of organic compounds as two enantiomeric forms. However chiral center alone is not sufficient condition for determination of optical activity.
The criteria to identify the optical activity are to look for absence of any symmetry element. The symmetry elements make any molecule optically inactive.

Want to see the full answer?
Check out a sample textbook solution
Chapter 8 Solutions
EBK STUDY GUIDE/SOLUTIONS MANUAL FOR OR
- Identify the missing organic reactants in the following reaction: X + Y H+ two steps Note: This chemical equation only focuses on the important organic molecules in the reaction. Additional inorganic or small-molecule reactants or products (like H2O) are not shown. In the drawing area below, draw the skeletal ("line") structures of the missing organic reactants X and Y. You may draw the structures in any arrangement that you like, so long as they aren't touching. Click and drag to start drawing a structure. Х :arrow_forwardDraw the mechanism of friedel-crafts acylation using acetyl chloride of m-Xylenearrow_forwardI need help naming these in IUPACarrow_forward
- H R Part: 1/2 :CI: is a/an electrophile Part 2 of 2 Draw the skeletal structure of the product(s) for the Lewis acid-base reaction. Include lone pairs and formal charges (if applicable) on the structures. 4-7: H ö- H Skip Part Check X :C1: $ % L Fi Click and drag to start drawing a structure. MacBook Pro & ㅁ x G 0: P Add or increase positive formal cha Save For Later Submit ©2025 McGraw Hill LLC. All Rights Reserved. Terms of Use | Privacy Centearrow_forwardDraw the friedel-crafts acylation mechanism of m-Xylenearrow_forwardDon't used hand raiting and don't used Ai solutionarrow_forward
- 1. Base on this experimental results, how do you know that the product which you are turning in is methyl 3-nitrobenzoate(meta substituted product ) rather than either of the other two products? 2. What observation suggests that at least a small amount of one or both of the other two isomers are in the mother liquor?arrow_forwardExplain Huckel's rule.arrow_forwardhere is my question can u help me please!arrow_forward
- Chemistry: The Molecular ScienceChemistryISBN:9781285199047Author:John W. Moore, Conrad L. StanitskiPublisher:Cengage LearningOrganic ChemistryChemistryISBN:9781305580350Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. FootePublisher:Cengage LearningChemistry & Chemical ReactivityChemistryISBN:9781337399074Author:John C. Kotz, Paul M. Treichel, John Townsend, David TreichelPublisher:Cengage Learning
- Chemistry & Chemical ReactivityChemistryISBN:9781133949640Author:John C. Kotz, Paul M. Treichel, John Townsend, David TreichelPublisher:Cengage Learning




