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OWLv2 for Masterton/Hurley's Chemistry: Principles and Reactions, 8th Edition, [Instant Access], 1 term (6 months)
8th Edition
ISBN: 9781305079311
Author: William L. Masterton; Cecile N. Hurley
Publisher: Cengage Learning US
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Question
Chapter 23, Problem 36QAP
(a)
Interpretation Introduction
Interpretation:
The difference between linear and branched polyethylene needs to be explained.
Concept Introduction:
A polymer is a long chain molecule made of large number of monomer units. The monomer is repeating units of a polymer that are linked to each other to produce a molecule of polymer.
These monomer units are linked to each other either through the formation of peptide linkage or glycosidic linkage or by removal of any moiety such as a water molecule.
Polyvinyl chloride, Bakelite and polystyrene are some of the example of
(b)
Interpretation Introduction
Interpretation:
The difference between glucose and fructose needs to be explained.
Concept Introduction:
Glucose and fructose are monosaccharideswith molecular formula C6H12O6. Glucose is also known as aldohexose consisting of 6 carbon atom and an
On the other hand, fructose is a ketohexose consisting 6 carbon atoms and a
(c)
Interpretation Introduction
Interpretation:
The difference between maltose and sucrose needs to be explained.
Concept Introduction:
Maltose and sucrose both are disaccharide with molecular formula C12H22O11. Maltose consists of 2 molecules of glucose while sucrose contains 1 molecule of glucose and 1 molecule of fructose in it.
These are disaccharide which consists of carbon, hydrogen and oxygen atoms only.
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Students have asked these similar questions
A student suggests that the molecule on the right can be made from a single molecule that doesn't have a ring. If the student is correct, draw the starting
material below, otherwise, check the box under the drawing area.
Click and drag to start
drawing a structure.
: ☐
+
NaOH
टे
Rate = k [I]1.7303[S2O82-]0.8502,
Based on your rate, write down a mechanism consistent with your results and indicate which step is the rate determining step.
36. Give the major product(s) of each of the following reactions. Aqueous work-up steps (when necessary) have
been omitted.
a. CH3CH=CHCH3
b.
CH3CH2CH2CCH3
H,PO₂, H₂O, A
(Hint: See Section 2-2.)
1. LIAIH. (CH,CH,),O
2. H', H₂O
H
NaBH, CH,CH₂OH
d.
Br
LIAIH. (CH,CH,)₂O
f.
CH3
NaBH, CH,CH,OH
(CH3)2CH
H
NaBH, CH,CH₂OH
H
Chapter 23 Solutions
OWLv2 for Masterton/Hurley's Chemistry: Principles and Reactions, 8th Edition, [Instant Access], 1 term (6 months)
Ch. 23 - Prob. 1QAPCh. 23 - Prob. 2QAPCh. 23 - Prob. 3QAPCh. 23 - Prob. 4QAPCh. 23 - Prob. 5QAPCh. 23 - Prob. 6QAPCh. 23 - Prob. 7QAPCh. 23 - Prob. 8QAPCh. 23 - Prob. 9QAPCh. 23 - Prob. 10QAP
Ch. 23 - Prob. 11QAPCh. 23 - Prob. 12QAPCh. 23 - Prob. 13QAPCh. 23 - Prob. 14QAPCh. 23 - Prob. 15QAPCh. 23 - Prob. 16QAPCh. 23 - Prob. 17QAPCh. 23 - Prob. 18QAPCh. 23 - Prob. 19QAPCh. 23 - Prob. 20QAPCh. 23 - How many chiral carbon atoms are there in ...Ch. 23 - How many chiral carbon atoms are there in sucrose?...Ch. 23 - Prob. 23QAPCh. 23 - Give the structural formulas of two different...Ch. 23 - (a) How many tripeptides can be made from glycine,...Ch. 23 - Prob. 26QAPCh. 23 - Prob. 27QAPCh. 23 - Prob. 28QAPCh. 23 - For alanine, Ka1=5.1105,Ka2=1.81010 . Calculate...Ch. 23 - Prob. 30QAPCh. 23 - On complete hydrolysis, a polypeptide gives two...Ch. 23 - Prob. 32QAPCh. 23 - Prob. 33QAPCh. 23 - Prob. 34QAPCh. 23 - Prob. 35QAPCh. 23 - Prob. 36QAPCh. 23 - Prob. 37QAPCh. 23 - Prob. 38QAPCh. 23 - Prob. 39QAPCh. 23 - Prob. 40QAPCh. 23 - Prob. 41QAPCh. 23 - Sketch the form in which leucine would exist in...Ch. 23 - How many tripeptides could one make from glycine,...Ch. 23 - A 1.00-mg sample of a pure protein yielded on...Ch. 23 - Describe what is meant by (a) the primary...Ch. 23 - Glycolysis is the process by which glucose is...Ch. 23 - Plants synthesize carbohydrates from CO2 and H2O...Ch. 23 - Prob. 48QAPCh. 23 - Prob. 49QAPCh. 23 - Prob. 50QAPCh. 23 - Prob. 51QAPCh. 23 - Aspartic acid acts as a triprotic acid with...
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- Predict the major products of this reaction: + H excess NaOH Δ ? Note that the second reactant is used in excess, that is, there is much more of the second reactant than the first. If there won't be any products, just check the box under the drawing area instead.arrow_forwardAn organic chemistry Teaching Assistant (TA) suggested in your last discussion section that there is only one major organic product of the following reaction and that this reaction builds a ring. If the TA is right, draw the product in the drawing area below. If the TA is wrong, just check the box below the drawing area. 1. NaOMe CH3O N. OCH3 ? 2. H3O+arrow_forwardComplete the reaction in the drawing area below by adding the major products to the right-hand side. If there won't be any products, because nothing will happen under these reaction conditions, check the box under the drawing area instead. Note: if the products contain one or more pairs of enantiomers, don't worry about drawing each enantiomer with dash and wedge bonds. Just draw one molecule to represent each pair of enantiomers, using line bonds at the chiral center. + More... ☐ ☐ : ☐ + G 1. NaOMe Click and drag to start drawing a structure. 2. H +arrow_forward
- 6. Ammonia reacts with nitrogen monoxide and oxygen to form nitrogen and water vapor. If the rate of consumption of NO is 4.5 mollitermin) (a) Find the rate of reaction (b) Find the rate of formations of N; and HO (c) Find the rate of consumption of NH, and O 4NH: 4NO 0:4: +60arrow_forward34. Give the expected major product of each of the following reactions. Conc. HI a. CH3CH2CH2OH b. (CH3)2CHCH2CH2OH Conc. HBr H Conc. HI C. OH Conc.HCI d. (CH3CH2)3COHarrow_forward42. Which of the following halogenated compounds can be used successfully to prepare a Grignard reagent for alcohol synthesis by subsequent reaction with an aldehyde or ketone? Which ones cannot and why? H3C CH3 a. Br H OH b. Cl C. I H H d. Cl e. H OCH3 Br Harrow_forward
- For each reaction below, decide if the first stable organic product that forms in solution will create a new CC bond, and check the appropriate box. Next, for each reaction to which you answered "Yes" to in the table, draw this product in the drawing area below. Note for advanced students: for this problem, don't worry if you think this product will continue to react under the current conditions - just focus on the first stable product you expect to form in solution. ? Will the first MgBr product that forms in this reaction create a new CC bond? olo ? OH جمله O Yes Ⓒ No MgCl ? Will the first product that forms in this reaction create a new CC bond? Click and drag to start drawing a structure. Yes No X ☐ : ☐ टे PHarrow_forwardAssign all the protonsarrow_forwardPROPOSE REACTION MECHANISM FOR ACID-CATALYZED REACTION OF 3-PENTANONE WITH DIMETHYLAMINEarrow_forward
- Assign all the protonsarrow_forwardAssign all the carbonsarrow_forward9 7 8 C 9 8 200 190 B 5 A -197.72 9 8 7 15 4 3 0: ང་ 200 190 180 147.52 134.98 170 160 150 140 130 120 110 100 90 90 OH 10 4 3 1 2 -143.04 140. 180 170 160 150 140 130 120 110 100 90 CI 3 5 1 2 141.89 140.07 200 190 180 170 160 150 140 130 120 110 100 ៖- 90 129. 126.25 80 70 60 -60 50 40 10 125.19 -129.21 80 70 3.0 20 20 -8 60 50 10 ppm -20 40 128.31 80 80 70 60 50 40 40 -70.27 3.0 20 10 ppm 00˚0-- 77.17 30 20 20 -45.36 10 ppm -0.00 26.48 22.32 ―30.10 ―-0.00arrow_forward
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