EBK CHEMISTRY FOR CHANGING TIMES
14th Edition
ISBN: 8220100663482
Author: MCCREARY
Publisher: PEARSON
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Question
Chapter 18, Problem 44P
Interpretation Introduction
Interpretation:
Functioning of cisplatin should be explained.
Concept Introduction:
- Cisplatin is an anticancer drug which can be classified as an alkylating agent.
- It is cis-diamminedichloroplatinum(II), cis
- It is given intravenously.
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Solution
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Use retrosynthetic analysis to suggest two paths to synthesize 2-methyl-3-hexanol using the Grignard reaction. (Click and drag
the appropriate image to the correct position in the reactions.)
Route 1
Aldehyde 1
or
+98
Aldehyde 2
Route 2
Q6
+100
Solved in 1 attempt
Q7
+95
Solved in 2 attempts
Q8
+98
Unlimited attempts
possible
+
+
Grignard 1
OH
H3O+
Grignard 2
Answer Bank
Q9
+90
MgBr
Unlimited attempts
possible
CH3CH2CH2MgBr
Q10
Unlimited attempts
Q11
?
?
+100
in 1 attempt
2-methyl-3-hexanol
CH3CH2MgBr
H
H
о
H
Attempt 3
2) (4 pt) After the reaction was completed, the student collected the following data. Crude
product data is the data collected after the reaction is finished, but before the product
is purified. "Pure" product data is the data collected after attempted purification using
recrystallization.
Student B's data:
Crude product data
"Pure"
product data
after
recrystallization
Crude mass: 0.93 g grey solid
Crude mp: 96-106 °C
Crude % yield:
Pure mass: 0.39 g white solid
Pure mp: 111-113 °C
Pure % yield:
a) Calculate the crude and pure percent yields for the student's reaction.
b) Summarize what is indicated by the crude and pure melting points.
Don't used hand raiting
Chapter 18 Solutions
EBK CHEMISTRY FOR CHANGING TIMES
Ch. 18 - Prob. 1RQCh. 18 - Prob. 2RQCh. 18 - Prob. 3RQCh. 18 - Prob. 4RQCh. 18 - Prob. 5RQCh. 18 - Prob. 6RQCh. 18 - What are prostaglandins? How do prostaglandins...Ch. 18 - Prob. 8RQCh. 18 - Prob. 9RQCh. 18 - Describe a synergistic effect involving drugs.
Ch. 18 - Prob. 11RQCh. 18 - Prob. 12RQCh. 18 - Prob. 13RQCh. 18 - Prob. 14RQCh. 18 - Prob. 15RQCh. 18 - Prob. 16RQCh. 18 - Prob. 17PCh. 18 - Classify the following drugs as natural,...Ch. 18 - Prob. 19PCh. 18 - Prob. 20PCh. 18 - Prob. 21PCh. 18 - Prob. 22PCh. 18 - Prob. 23PCh. 18 - Prob. 24PCh. 18 - Prob. 25PCh. 18 - Prob. 26PCh. 18 - Which of the following was originally marketed as...Ch. 18 - Prob. 28PCh. 18 - Which of the following is not considered to be an...Ch. 18 - How does heroin differ from morphine in its...Ch. 18 - Prob. 31PCh. 18 - How are endorphins related to (a) the anesthetic...Ch. 18 - Prob. 33PCh. 18 - Prob. 34PCh. 18 - Prob. 35PCh. 18 - Prob. 36PCh. 18 - Prob. 37PCh. 18 - Prob. 38PCh. 18 - Prob. 39PCh. 18 - Prob. 40PCh. 18 - Prob. 41PCh. 18 - Prob. 42PCh. 18 - Prob. 43PCh. 18 - Prob. 44PCh. 18 - Prob. 45PCh. 18 - Prob. 46PCh. 18 - Give three differences between hormones and...Ch. 18 - Prob. 48PCh. 18 - Prob. 49PCh. 18 - Prob. 50PCh. 18 - Prob. 51PCh. 18 - Prob. 52PCh. 18 - Prob. 53PCh. 18 - Prob. 54PCh. 18 - Prob. 55PCh. 18 - Prob. 56PCh. 18 - Prob. 57PCh. 18 - Which of the following is often treated with...Ch. 18 - Prob. 59PCh. 18 - Prob. 60PCh. 18 - Prob. 61PCh. 18 - Prob. 62PCh. 18 - Prob. 63PCh. 18 - Prob. 64PCh. 18 - Prob. 65PCh. 18 - Prob. 66PCh. 18 - Prob. 67PCh. 18 - What is an agonist? What is an antagonist?Ch. 18 - Prob. 69PCh. 18 - Prob. 70PCh. 18 - Prob. 71PCh. 18 - What is the difference between drug abuse and drug...Ch. 18 - Review the information on structure and function...Ch. 18 - Prob. 74APCh. 18 - Prob. 75APCh. 18 - Prob. 76APCh. 18 - Prob. 77APCh. 18 - Prob. 78APCh. 18 - Prob. 79APCh. 18 - Prob. 80APCh. 18 - Prob. 81APCh. 18 - Prob. 82APCh. 18 - Prob. 83APCh. 18 - Prob. 84APCh. 18 - Prob. 85APCh. 18 - Prob. 86APCh. 18 - Prob. 87APCh. 18 - Prob. 88APCh. 18 - Prob. 89APCh. 18 - Prob. 90APCh. 18 - Prob. 91APCh. 18 - Prob. 92APCh. 18 - Prob. 93APCh. 18 - Prob. 94APCh. 18 - Prob. 95APCh. 18 - Which of the following compounds are classified as...Ch. 18 - Prob. 97APCh. 18 - Prob. 98APCh. 18 - Prob. 99APCh. 18 - Prob. 100APCh. 18 - Prob. 101APCh. 18 - Prob. 102APCh. 18 - Prob. 103APCh. 18 - Prob. 104APCh. 18 - Prob. 18.1CTECh. 18 - Prob. 18.2CTECh. 18 - Prob. 18.3CTECh. 18 - Prob. 18.4CTECh. 18 - Prob. 18.5CTECh. 18 - Prob. 18.6CTECh. 18 - Prob. 18.7CTECh. 18 - Prob. 18.8CTECh. 18 - Prob. 1CGPCh. 18 - Prob. 2CGPCh. 18 - Prob. 3CGPCh. 18 - Prob. 4CGPCh. 18 - Prob. 5CGPCh. 18 - Prob. 6CGPCh. 18 - Prob. 7CGPCh. 18 - Prob. 8CGPCh. 18 - Prob. 9CGPCh. 18 - Prob. 10CGPCh. 18 - Prob. 11CGPCh. 18 - Prob. 12CGPCh. 18 - Prob. 13CGPCh. 18 - Prob. 14CGPCh. 18 - Prob. 1CHQCh. 18 - Prob. 2CHQCh. 18 - Prob. 3CHQ
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- A DEPT NMR spectrum is shown for a molecule with the molecular formula of C5H12O. Draw the structure that best fits this data. 200 180 160 140 120 100 一盆 00 40 8- 20 ppm 0 Qarrow_forwardDon't used hand raitingarrow_forwardShown below is the major resonance structure for a molecule. Draw the second best resonance structure of the molecule. Include all non-zero formal charges. H. H. +N=C H H H Cl: Click and drag to start drawing a structure. : ? g B S olo Ar B Karrow_forward
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