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Pearson eText for Essential Organic Chemistry -- Instant Access (Pearson+)
3rd Edition
ISBN: 9780137533268
Author: Paula Bruice
Publisher: PEARSON+
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Textbook Question
Chapter 9, Problem 55P
Triethylenemelamine (TEM) is an antitumor agent. Its activity is due to its ability to cross-link DNA
- a. Explain why it can be used only under slightly acidic conditions.
- b. Explain why it can cross-link DNA.
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1. The Ability of a substance to exist in different crystalline form
a. Lattice
b. Polymorphism
c. Crystallization
d. Amphoterism
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b. Protein unbound
c. Free drug
d. Both B & C
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d. Solubility decrease with decrease surface area
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b. Potency
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d. Area under the curve
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c. Gene Transcription linked receptor
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c. No effect
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a. Faster
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22. Your 9 year-old son wants to show his friends how cool he is. So he designs an
experiment that makes his friends' tee shirts "magically' turn black, metallic green. The
caused this color change.
presence of
and
a. sucrose, neutral red
b. glucose. Phenol red
c. lactose, eosin methylene blue
d. lactose, neutral red
e. glucose, eosin methylene blue
23. Your husband is fully amazed when his dinner plate "magically" turned black when
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a. iron, amylase
b. trypthophan, indole
c. iron, hydrogen sulfide
d. lipase, fats
e. decarboxylase, indole
24. The role of safranin in the gram stain is similar to the role of
fast stain.
a. methylene blue
b. carbolfuschin
c. acetone alcohol
d. heat
e. crystal violet
25. Immersion oil was used in conjunction with the
the spread of light to increase the microscope's resolution.
a. 100x, condensed
b. 40x, increased
c. 100x total magnification, increased…
Chapter 9 Solutions
Pearson eText for Essential Organic Chemistry -- Instant Access (Pearson+)
Ch. 9.1 - Draw the structures of straight-chain alcohols...Ch. 9.1 - Prob. 2PCh. 9.1 - Prob. 3PCh. 9.2 - Why are NH3 and CH3NH2 no longer nucleophiles when...Ch. 9.2 - Prob. 5PCh. 9.2 - The observed relative reactivities of primary,...Ch. 9.4 - Which of the following alcohols would dehydrate...Ch. 9.4 - Prob. 10PCh. 9.4 - Prob. 11PCh. 9.4 - Prob. 12P
Ch. 9.4 - Prob. 13PCh. 9.5 - What product will be obtained from the reaction of...Ch. 9.5 - Prob. 15PCh. 9.6 - a. What is each ethers systematic name? 1....Ch. 9.8 - Draw the structure of the following: a....Ch. 9.8 - Prob. 20PCh. 9.8 - Would you expect the reactivity of a five-membered...Ch. 9.9 - Explain why the two arene oxides in Problem 22...Ch. 9.9 - Which compound is more likely to be...Ch. 9.11 - The following three nitrogen mustards were studied...Ch. 9 - What are the common and systematic names of the...Ch. 9 - Prob. 28PCh. 9 - Prob. 29PCh. 9 - Prob. 30PCh. 9 - Prob. 31PCh. 9 - What is the major product obtained from the...Ch. 9 - Draw structures for the following: a....Ch. 9 - Prob. 34PCh. 9 - Prob. 35PCh. 9 - Prob. 36PCh. 9 - Prob. 37PCh. 9 - Ethylene oxide reacts readily with HO.because of...Ch. 9 - Propose a mechanism for each of the following...Ch. 9 - Which of the following ethers would be obtained in...Ch. 9 - Show how each of the following syntheses could be...Ch. 9 - Prob. 42PCh. 9 - Prob. 43PCh. 9 - Prob. 44PCh. 9 - Propose a mechanism for each of the following...Ch. 9 - a. Propose a mechanism for the following reaction:...Ch. 9 - Three arene oxides can be obtained from...Ch. 9 - Prob. 48PCh. 9 - The following reaction takes place several times...Ch. 9 - Show how each of the following compounds could be...Ch. 9 - Propose a mechanism for the following reaction:Ch. 9 - Propose a mechanism for the following reaction:Ch. 9 - What alkenes would you expect to be obtained from...Ch. 9 - Triethylenemelamine (TEM) is an antitumor agent....Ch. 9 - When a diol that has OH groups on adjacent carbons...Ch. 9 - What product is obtained when...Ch. 9 - Prob. 58P
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