Chemistry
10th Edition
ISBN:9781305957404
Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Publisher:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Chapter1: Chemical Foundations
Section: Chapter Questions
Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...
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![9:13 i O
NI all 30%
PART A: Ciprofibrate (C13H14CI203)
1. Draw the structure and write the IUPAC name of a drug assigned to you (use Chemsketch software).
HO,
H,C CH,
2-14-(2,2-dichlorocyclopropyl)phenoxy}-2-methylpropanoicacid
2. Mention its two most important medicinal uses.
+ Hypertriglyceridemia
+ Low high-density lipoprotein (HDL)
3. Identify and name all the functional groups present in the molecule. Ciprofibrate
Carboxylic Acid - carbonyl - Arene - benzene ring - ether - alkyl chloride - alkyl halide - leaving group.
4. Label Chiral carbon atoms, if any.
PART B: m-dinitrobenzene
1. Draw the structure of organic compound assigned to you using Chemsketch.
m-dinitrobenzene
2. Name and Draw the structures of all possible chemical (Electrophilic aromatic substitution) reactions
of the compound namely; m-dinitrobenzene
a. Halogenation (Chlorination or Bromination)
II](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2F1e735b92-11f6-4204-abe0-0d934e258b23%2Fc7e67c42-cfca-4b10-8bf7-01d6bf026e05%2Fp97dh78_processed.jpeg&w=3840&q=75)
Transcribed Image Text:9:13 i O
NI all 30%
PART A: Ciprofibrate (C13H14CI203)
1. Draw the structure and write the IUPAC name of a drug assigned to you (use Chemsketch software).
HO,
H,C CH,
2-14-(2,2-dichlorocyclopropyl)phenoxy}-2-methylpropanoicacid
2. Mention its two most important medicinal uses.
+ Hypertriglyceridemia
+ Low high-density lipoprotein (HDL)
3. Identify and name all the functional groups present in the molecule. Ciprofibrate
Carboxylic Acid - carbonyl - Arene - benzene ring - ether - alkyl chloride - alkyl halide - leaving group.
4. Label Chiral carbon atoms, if any.
PART B: m-dinitrobenzene
1. Draw the structure of organic compound assigned to you using Chemsketch.
m-dinitrobenzene
2. Name and Draw the structures of all possible chemical (Electrophilic aromatic substitution) reactions
of the compound namely; m-dinitrobenzene
a. Halogenation (Chlorination or Bromination)
II
![9:13 i O
N ll 30%
2-(4-(2,2-dichlorocyclopropyl)phenoxy)-2-methylpropanoicacid
2. Mention its two most important medicinal uses.
+ Hypertriglyceridemia
+ Low high-density lipoprotein (HDL)
3. Identify and name all the functional groups present in the molecule. Ciprofibrate
Carboxylic Acid -carbonyl - Arene - benzene ring - ether - alkyl chloride - alkyl halide - leaving group.
4. Label Chiral carbon atoms, if any.
PART B: m-dinitrobenzene
1. Draw the structure of organic compound assigned to you using Chemsketch.
m-dinitrobenzene
2. Name and Draw the structures of all possible chemical (Electrophilic aromatic substitution) reactions
of the compound namely; m-dinitrobenzene
a. Halogenation (Chlorination or Bromination)
b. Nitration
c. Sulphonation
d. Friedal Craft Alkylation
e. Friedal Craft Acylation
II](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2F1e735b92-11f6-4204-abe0-0d934e258b23%2Fc7e67c42-cfca-4b10-8bf7-01d6bf026e05%2F5tbgno_processed.jpeg&w=3840&q=75)
Transcribed Image Text:9:13 i O
N ll 30%
2-(4-(2,2-dichlorocyclopropyl)phenoxy)-2-methylpropanoicacid
2. Mention its two most important medicinal uses.
+ Hypertriglyceridemia
+ Low high-density lipoprotein (HDL)
3. Identify and name all the functional groups present in the molecule. Ciprofibrate
Carboxylic Acid -carbonyl - Arene - benzene ring - ether - alkyl chloride - alkyl halide - leaving group.
4. Label Chiral carbon atoms, if any.
PART B: m-dinitrobenzene
1. Draw the structure of organic compound assigned to you using Chemsketch.
m-dinitrobenzene
2. Name and Draw the structures of all possible chemical (Electrophilic aromatic substitution) reactions
of the compound namely; m-dinitrobenzene
a. Halogenation (Chlorination or Bromination)
b. Nitration
c. Sulphonation
d. Friedal Craft Alkylation
e. Friedal Craft Acylation
II
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