EBK GENERAL, ORGANIC, AND BIOLOGICAL CH
3rd Edition
ISBN: 8220101460288
Author: Deal
Publisher: PEARSON
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Chapter 11, Problem 1IA.1Q
Summary Introduction
To name:
The three components of molecules found in
Introduction:
Nucleotide serves as basic building block of nucleic acid as it is composed of nitrogenous bases, pentose sugar and phosphate group. It is found in living cells. There are two types of
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In a reaction between two reactants A and B, the half-life is the same for both.(1) Only if the stoichiometry A:B is 1:1.(2) If the initial quantities of A and B are in their stoichiometric ratios.
There are 48 pairs of students in the following table. Each pair has quantitatively determined the mass of taurine in a 250 mL can of the popular energy drink marketed as “Munster” using High Performance Liquid Chromatography (HPLC). The class results are presented below:
QUESTION: Calculate the measurement of uncertainty and provide the data in a spreadsheet table.
Mass of Taurine (mg)
Mass of Taurine (mg)
(Table continued)
152.01
152.23
151.87
151.45
154.11
152.64
152.98
153.24
152.88
151.45
153.49
152.48
150.68
152.33
151.52
153.63
152.48
151.68
153.17
153.40
153.77
153.67
152.34
153.16
152.57
153.02
152.86
151.50
151.23
152.57
152.72
151.54
146.47
152.38
152.44
152.54
152.53
152.54
151.32
152.87
151.24
153.26
152.02
152.90
152.87
151.49
152.46
152.58
1. Predict the organic product(s) of the following reactions. Assume excess of reagents unless
otherwise noted.
a)
&l
BH3 •THF
b)
1) NaOH
2) H3O+
solve
d)
ala
1) EtMgBr
2) H3O+
e)
H2N
سكر
CuLi
NH2
1) SOCI2
2) EtMgBr
3) H3O+
NC
H3O+
Δ
Chapter 11 Solutions
EBK GENERAL, ORGANIC, AND BIOLOGICAL CH
Ch. 11 - Prob. 11.1PPCh. 11 - Prob. 11.2PPCh. 11 - Prob. 11.3PPCh. 11 - Prob. 11.4PPCh. 11 - Prob. 11.5PPCh. 11 - Which of the pentose sugars is found in DNA? Which...Ch. 11 - Prob. 11.7PPCh. 11 - Prob. 11.8PPCh. 11 - Prob. 11.9PPCh. 11 - Prob. 11.10PP
Ch. 11 - Prob. 11.11PPCh. 11 - Prob. 11.12PPCh. 11 - Draw the dinucleotide GC that would be found in...Ch. 11 - Prob. 11.14PPCh. 11 - Prob. 11.15PPCh. 11 - Prob. 11.16PPCh. 11 - Prob. 11.17PPCh. 11 - Prob. 11.18PPCh. 11 - Write the base sequence and label the 3 and 5 ends...Ch. 11 - Write the base sequence and label the 3 and 5 ends...Ch. 11 - Prob. 11.21PPCh. 11 - I jst the similarities and differences in the...Ch. 11 - Prob. 11.23PPCh. 11 - Prob. 11.24PPCh. 11 - Prob. 11.25PPCh. 11 - In your own words, define the term translation.Ch. 11 - Prob. 11.27PPCh. 11 - Prob. 11.28PPCh. 11 - Prob. 11.29PPCh. 11 - Prob. 11.30PPCh. 11 - Provide the three-letter amino-acid sequence...Ch. 11 - Provide the three-letter amino-acid sequence...Ch. 11 - Prob. 11.33PPCh. 11 - Prob. 11.34PPCh. 11 - The following portion of DNA is in the template...Ch. 11 - The following portion of DNA is in the template...Ch. 11 - Prob. 11.37PPCh. 11 - In your own words, define a silent mutation.Ch. 11 - Prob. 11.39PPCh. 11 - Consider the following portion of mRNA produced by...Ch. 11 - Prob. 11.41PPCh. 11 - Prob. 11.42PPCh. 11 - Why do viruses need to enter a host cell?Ch. 11 - Prob. 11.44PPCh. 11 - Prob. 11.45PPCh. 11 - It a virus contains viral RNA, a. name the first...Ch. 11 - Prob. 11.47PPCh. 11 - How do nucleoside analogs disrupt the life cycle...Ch. 11 - Prob. 11.49PPCh. 11 - Prob. 11.50PPCh. 11 - Prob. 11.51PPCh. 11 - Describe the structure of a plasmid.Ch. 11 - Prob. 11.53PPCh. 11 - Prob. 11.54PPCh. 11 - Prob. 11.55APCh. 11 - Prob. 11.56APCh. 11 - Prob. 11.57APCh. 11 - Prob. 11.58APCh. 11 - Prob. 11.59APCh. 11 - Prob. 11.60APCh. 11 - Prob. 11.61APCh. 11 - Write the complementary base sequence for each of...Ch. 11 - Prob. 11.63APCh. 11 - Prob. 11.64APCh. 11 - Prob. 11.65APCh. 11 - Prob. 11.66APCh. 11 - Prob. 11.67APCh. 11 - Prob. 11.68APCh. 11 - Prob. 11.69APCh. 11 - Prob. 11.70APCh. 11 - Prob. 11.71APCh. 11 - Endorphins arc polypeptides that reduce pain. What...Ch. 11 - What is the one-letter amino-acid sequence formed...Ch. 11 - Prob. 11.74APCh. 11 - What is the anticodon on tRNA for each of the...Ch. 11 - a. A base substitution changes a codon for an...Ch. 11 - Prob. 11.77APCh. 11 - Discuss whether or not each of the following is a...Ch. 11 - Prob. 11.79APCh. 11 - Prob. 11.80APCh. 11 - Prob. 11.81APCh. 11 - List two societal benefits to recombinant DNA...Ch. 11 - Prob. 11.83APCh. 11 - Oxytocin is a small peptide hormone involved in...Ch. 11 - Alpha-melanocyte stimulating hormone (o-MSH) is a...Ch. 11 - a. If the DNA chromosomes of salmon contain 28%...Ch. 11 - A protein aiumm 35 amino acids. How many...Ch. 11 - The DNA double helix can unwind or denature at...Ch. 11 - Prob. 1IA.1QCh. 11 - Prob. 1IA.2QCh. 11 - Prob. 1IA.3QCh. 11 - Prob. 1IA.4QCh. 11 - Prob. 1IA.5QCh. 11 - Prob. 1IA.6QCh. 11 - Prob. 1IA.7QCh. 11 - Prob. 1IA.8QCh. 11 - Prob. 1IA.9QCh. 11 - Prob. 2IA.1QCh. 11 - Prob. 2IA.2QCh. 11 - Prob. 2IA.3QCh. 11 - Prob. 3IA.1QCh. 11 - Prob. 3IA.2QCh. 11 - Prob. 3IA.3QCh. 11 - Prob. 3IA.4QCh. 11 - Prob. 3IA.5QCh. 11 - Prob. 3IA.6QCh. 11 - Prob. 3IA.7QCh. 11 - Prob. 3IA.8QCh. 11 - Prob. 3IA.9QCh. 11 - Prob. 3IA.10QCh. 11 - Prob. 1ICCh. 11 - Prob. 2ICCh. 11 - Prob. 3IC
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- There are 48 pairs of students in the following table. Each pair has quantitatively determined the mass of taurine in a 250 mL can of the popular energy drink marketed as “Munster” using High Performance Liquid Chromatography (HPLC). The class results are presented below: QUESTION: Summarise and report these results including an indication of measurement uncertainty. In both calculation samples calculate if an outlier is present, max value, number of samples, mean, standard deviation, g (suspect), g (critical) and t (critical). Mass of Taurine (mg) Mass of Taurine (mg) (Table continued) 152.01 152.23 151.87 151.45 154.11 152.64 152.98 153.24 152.88 151.45 153.49 152.48 150.68 152.33 151.52 153.63 152.48 151.68 153.17 153.40 153.77 153.67 152.34 153.16 152.57 153.02 152.86 151.50 151.23 152.57 152.72 151.54 146.47 152.38 152.44 152.54 152.53 152.54 151.32…arrow_forwardIndicate the rate expressions for reactions that have order 0, 1, and 2.arrow_forwardPROBLEMS Q1) Label the following salts as either acidic, basic, or neutral a) Fe(NOx) c) AlBr b) NH.CH COO d) HCOON (1/2 mark each) e) Fes f) NaBr Q2) What is the pH of a 0.0750 M solution of sulphuric acid?arrow_forward
- 8. Draw all the resonance forms for each of the fling molecules or ions, and indicate the major contributor in each case, or if they are equivalent (45) (2) -PH2 سمة مدarrow_forwardA J то گای ه +0 Also calculate the amount of starting materials chlorobenzaldehyde and p-chloroacetophenone required to prepare 400 mg of the given chalcone product 1, 3-bis(4-chlorophenyl)prop-2-en-1-one molar mass ok 1,3-bis(4-Chlorophenyl) prop-2-en-1-one = 277.1591m01 number of moles= 0.400/277.15 = 0.00144 moles 2 x 0.00 144=0.00288 moves arams of acetophenone = 0.00144 X 120.16 = 0.1739 0.1739x2=0.3469 grams of benzaldehyde = 0.00144X106.12=0.1539 0.1539x2 = 0.3069 Starting materials: 0.3469 Ox acetophenone, 0.3069 of benzaldehyde 3arrow_forward1. Answer the questions about the following reaction: (a) Draw in the arrows that can be used make this reaction occur and draw in the product of substitution in this reaction. Be sure to include any relevant stereochemistry in the product structure. + SK F Br + (b) In which solvent would this reaction proceed the fastest (Circle one) Methanol Acetone (c) Imagine that you are working for a chemical company and it was your job to perform a similar reaction to the one above, with the exception of the S atom in this reaction being replaced by an O atom. During the reaction, you observe the formation of three separate molecules instead of the single molecule obtained above. What is the likeliest other products that are formed? Draw them in the box provided.arrow_forward
- 3. For the reactions below, draw the arrows corresponding to the transformations and draw in the boxes the reactants or products as indicated. Note: Part A should have arrows drawn going from the reactants to the middle structure and the arrows on the middle structure that would yield the final structure. For part B, you will need to draw in the reactant before being able to draw the arrows corresponding to product formation. A. B. Rearrangement ΘΗarrow_forward2. Draw the arrows required to make the following reactions occur. Please ensure your arrows point from exactly where you want to exactly where you want. If it is unclear from where arrows start or where they end, only partial credit will be given. Note: You may need to draw in lone pairs before drawing the arrows. A. B. H-Br 人 C Θ CI H Cl Θ + Br Oarrow_forward4. For the reactions below, draw the expected product. Be sure to indicate relevant stereochemistry or formal charges in the product structure. a) CI, H e b) H lux ligh Br 'Harrow_forward
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