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(a)
Interpretation:
The names of
Concept introduction:
Functional groups are atom or groups of atoms which are responsible for special chemical or physical properties of the molecule. IUPAC purposed a complete list of different functional groups with their prefix and suffix which can be used in the naming of the molecule. Some of the atoms can act as functional group such as −Cl, -F, -Br etc whereas some of them are groups of atoms like −NH2, -NO2, -OH etc.
(b)
Interpretation:
Identify the hybridization of
Concept introduction:
Hybridization is the process of mixing of atomic orbitals to form same energy and same shape hybrid orbitals which form covalent bond with overlapping of atomic orbitals of other atoms. The number of
(c)
Interpretation:
Identify the chiral C atoms in ephedrine.
Concept introduction:
A chiral carbon atom is the carbon atom which is bonded with four different atoms or group of atoms. The presence of chiral carbon atom makes that molecule optically active so it can rotate the plane polarized light either clockwise or anti-clockwise. Such molecules are called as optically active molecule and two different configuration of same molecule are called as enantiomers. They are non-superimposable mirror images of each other.
(d)
Interpretation:
Calculate the pKb value for ephedrine with the help of given information.
Concept introduction:
Ephedrine is a weak base which is mainly used as a center nervous system stimulant. Since it acts as a weak base therefore it gives OH- ions in its aqueous solution.
The base dissociation constant
The relation between
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Chapter 26 Solutions
GENERAL CHEMISTRY(LL)-W/MASTERINGCHEM.
- 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
- ChemistryChemistryISBN:9781305957404Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCostePublisher:Cengage LearningChemistry: An Atoms First ApproachChemistryISBN:9781305079243Author:Steven S. Zumdahl, Susan A. ZumdahlPublisher:Cengage Learning
- Chemistry: The Molecular ScienceChemistryISBN:9781285199047Author:John W. Moore, Conrad L. StanitskiPublisher:Cengage LearningChemistry: Matter and ChangeChemistryISBN:9780078746376Author:Dinah Zike, Laurel Dingrando, Nicholas Hainen, Cheryl WistromPublisher:Glencoe/McGraw-Hill School Pub CoChemistry & Chemical ReactivityChemistryISBN:9781337399074Author:John C. Kotz, Paul M. Treichel, John Townsend, David TreichelPublisher:Cengage Learning
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