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Bundle: Chemistry: The Molecular Science, 5th, Loose-Leaf + OWLv2 with Quick Prep 24-Months Printed Access Card
5th Edition
ISBN: 9781305367487
Author: John W. Moore, Conrad L. Stanitski
Publisher: Cengage Learning
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Question
Chapter 2, Problem 128QRT
(a)
Interpretation Introduction
Interpretation:
The given name for the formula
(b)
Interpretation Introduction
Interpretation:
The given name for the formula
.
(c)
Interpretation Introduction
Interpretation:
The given name for the formula
(d)
Interpretation Introduction
Interpretation:
The given name for the formula
(e)
Interpretation Introduction
Interpretation:
The given name for the formula
(f)
Interpretation Introduction
Interpretation:
The given name for the formula
Expert Solution & Answer
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Students have asked these similar questions
Complete the following table. The only density needed is already given. Show your
calculations in a neat and easy-to-follow manner in the space below the table. All units
should be included and significant figures should be given close attention. Be sure to notice
that the amount of material should be in millimoles rather than moles, and the theoretical
mass of the product should in milligrams rather than grams.
LOCH 3
+
H2SO4
HNO 3
O=C-OCH 3
NO2
x
H₂O
F.W.
4.0 mL 1.3 M
amount
0.50 mL
in H2SO4
mg Theoretical
Theoretical
mmoles
density
1.09
Kumada Coupling:
1. m-Diisobutylbenzene below could hypothetically be synthesized by Friedel-Crafts reaction. Write out the reaction with a
mechanism and give two reasons why you would NOT get the desired product.
Draw the reaction (NOT a mechanism) for a Kumada coupling to produce the molecule above from m-dichlorobenzene.
Calculate the theoretical yield for the reaction in question 2 using 1.5 g of p-dichlorobenzene and 3.0 mL isobutyl bromide.
What signals appeared/disappeared/shifted that indicate that you have your intended product and not starting material? What
other impurities are present in your product and how do you know?
Wintergreen from Aspirin:
1. In isolating the salicylic acid, why is it important to press out as much of the water as possible?
2. Write the mechanism of the esterification reaction you did.
3.
What characteristic absorption band changes would you expect in the IR spectrum on going from aspirin to salicyclic acid and
then to methyl salicylate as you did in the experiment today? Give approximate wavenumbers associated with each functional
group change.
What signals appeared/disappeared/shifted that indicate that you have your intended product and not starting material? What
other impurities are present in your product and how do you know?
Chapter 2 Solutions
Bundle: Chemistry: The Molecular Science, 5th, Loose-Leaf + OWLv2 with Quick Prep 24-Months Printed Access Card
Ch. 2.1 - When you comb your hair on a dry day, your hair...Ch. 2.2 - Prob. 2.1PSPCh. 2.2 - Prob. 2.2PSPCh. 2.2 - Prob. 2.2CECh. 2.2 - Prob. 2.3PSPCh. 2.3 - Prob. 2.4PSPCh. 2.3 - A student in your chemistry class tells you that...Ch. 2.3 - Prob. 2.5PSPCh. 2.3 - Prob. 2.4CECh. 2.3 - Prob. 2.5CE
Ch. 2.4 - Prob. 2.6PSPCh. 2.4 - Prob. 2.6CECh. 2.4 - Prob. 2.7PSPCh. 2.4 - Prob. 2.8PSPCh. 2.5 - Prob. 2.9PSPCh. 2.5 - Prob. 2.10PSPCh. 2.6 - Prob. 2.7CECh. 2.7 - Prob. 2.8CECh. 2.7 - Prob. 2.11PSPCh. 2.7 - Prob. 2.9ECh. 2.8 - Prob. 2.12PSPCh. 2.8 - Prob. 2.10ECh. 2.9 - Prob. 2.11ECh. 2.9 - Prob. 2.12ECh. 2.9 - Prob. 2.13CECh. 2.9 - According to Table 2.10, five constitutional...Ch. 2.11 - Calculate (a) the amount of Ti atoms in 4.00 g...Ch. 2.11 - Prob. 2.15CECh. 2.11 - Prob. 2.16ECh. 2.11 - Prob. 2.17CECh. 2.11 - Prob. 2.18ECh. 2.11 - Prob. 2.19ECh. 2.11 - Prob. 2.14PSPCh. 2.11 - Prob. 2.15PSPCh. 2.11 - Prob. 2.16PSPCh. 2.11 - Prob. 2.20CECh. 2.12 - Prob. 2.17PSPCh. 2.12 - Prob. 2.18PSPCh. 2.12 - Prob. 2.21ECh. 2.12 - Hydrazine is composed of 87.42% nitrogen and...Ch. 2.12 - Prob. 2.20PSPCh. 2.12 - Prob. 2.22ECh. 2 - An isotope of an element contains 63 protons and...Ch. 2 - Prob. IISPCh. 2 - Prob. IIISPCh. 2 - Dioxathion, a pesticide, contains carbon,...Ch. 2 - Prob. 1QRTCh. 2 - Prob. 2QRTCh. 2 - Prob. 3QRTCh. 2 - Prob. 4QRTCh. 2 - Prob. 5QRTCh. 2 - Prob. 6QRTCh. 2 - Prob. 7QRTCh. 2 - Prob. 8QRTCh. 2 - Prob. 9QRTCh. 2 - Prob. 10QRTCh. 2 - Match these by placing the correct notation in the...Ch. 2 - Prob. 12QRTCh. 2 - Prob. 13QRTCh. 2 - Prob. 14QRTCh. 2 - Prob. 15QRTCh. 2 - Prob. 16QRTCh. 2 - Prob. 17QRTCh. 2 - Prob. 18QRTCh. 2 - Prob. 19QRTCh. 2 - Prob. 20QRTCh. 2 - Prob. 21QRTCh. 2 - Prob. 22QRTCh. 2 - Prob. 23QRTCh. 2 - Prob. 24QRTCh. 2 - Prob. 25QRTCh. 2 - Prob. 26QRTCh. 2 - Prob. 27QRTCh. 2 - Prob. 28QRTCh. 2 - Argon has three naturally occurring isotopes:...Ch. 2 - Prob. 30QRTCh. 2 - Prob. 31QRTCh. 2 - Prob. 32QRTCh. 2 - Prob. 33QRTCh. 2 - Prob. 34QRTCh. 2 - Prob. 35QRTCh. 2 - Prob. 36QRTCh. 2 - Prob. 37QRTCh. 2 - Prob. 38QRTCh. 2 - Prob. 39QRTCh. 2 - Prob. 40QRTCh. 2 - Prob. 41QRTCh. 2 - Prob. 42QRTCh. 2 - Prob. 43QRTCh. 2 - Prob. 44QRTCh. 2 - Prob. 45QRTCh. 2 - Prob. 46QRTCh. 2 - Prob. 47QRTCh. 2 - Prob. 48QRTCh. 2 - Prob. 49QRTCh. 2 - Prob. 50QRTCh. 2 - Prob. 51QRTCh. 2 - Prob. 52QRTCh. 2 - Prob. 53QRTCh. 2 - Prob. 54QRTCh. 2 - Prob. 55QRTCh. 2 - Prob. 56QRTCh. 2 - Prob. 57QRTCh. 2 - Prob. 58QRTCh. 2 - Prob. 59QRTCh. 2 - Prob. 60QRTCh. 2 - Prob. 61QRTCh. 2 - Prob. 62QRTCh. 2 - Prob. 63QRTCh. 2 - Prob. 64QRTCh. 2 - Prob. 65QRTCh. 2 - Prob. 66QRTCh. 2 - Prob. 67QRTCh. 2 - Prob. 68QRTCh. 2 - Prob. 69QRTCh. 2 - Prob. 70QRTCh. 2 - Prob. 71QRTCh. 2 - Prob. 72QRTCh. 2 - Prob. 73QRTCh. 2 - Prob. 74QRTCh. 2 - If you have a ring that contains 1.94 g gold,...Ch. 2 - You have a pure sample of the antiseptic...Ch. 2 - You have a pure sample of apholate, C12H24N9P3, a...Ch. 2 - Prob. 78QRTCh. 2 - Prob. 79QRTCh. 2 - Prob. 80QRTCh. 2 - Prob. 81QRTCh. 2 - Prob. 82QRTCh. 2 - Prob. 83QRTCh. 2 - Prob. 84QRTCh. 2 - Prob. 85QRTCh. 2 - Prob. 86QRTCh. 2 - Prob. 87QRTCh. 2 - Prob. 88QRTCh. 2 - Prob. 89QRTCh. 2 - Prob. 90QRTCh. 2 - Quinine (molar mass = 324.41 g/mol) is used as a...Ch. 2 - Prob. 92QRTCh. 2 - The mineral uraninite is a uranium oxide that is...Ch. 2 - Carbonic anhydrase, an important enzyme in...Ch. 2 - Nitrogen fixation in the root nodules of peas and...Ch. 2 - Disilane, Si2Hx, contains 90.28% silicon by mass....Ch. 2 - Chalky, white crystals in mineral collections are...Ch. 2 - A well-known reagent in analytical chemistry,...Ch. 2 - Prob. 99QRTCh. 2 - Prob. 100QRTCh. 2 - The density of a solution of sulfuric acid is...Ch. 2 - Prob. 102QRTCh. 2 - Prob. 103QRTCh. 2 - Prob. 104QRTCh. 2 - Prob. 105QRTCh. 2 - Prob. 106QRTCh. 2 - Prob. 107QRTCh. 2 - The Statue of Liberty in New York harbor is made...Ch. 2 - Prob. 109QRTCh. 2 - Prob. 110QRTCh. 2 - Prob. 111QRTCh. 2 - Prob. 112QRTCh. 2 - Prob. 113QRTCh. 2 - Prob. 114QRTCh. 2 - Prob. 115QRTCh. 2 - Prob. 116QRTCh. 2 - Prob. 117QRTCh. 2 - Prob. 118QRTCh. 2 - Prob. 119QRTCh. 2 - Prob. 120QRTCh. 2 - Prob. 121QRTCh. 2 - Prob. 122QRTCh. 2 - Prob. 123QRTCh. 2 - Prob. 124QRTCh. 2 - Prob. 125QRTCh. 2 - Prob. 126QRTCh. 2 - Prob. 127QRTCh. 2 - Prob. 128QRTCh. 2 - Prob. 129QRTCh. 2 - The element bromine is Br2, so the mass of a Br2...Ch. 2 - Uranium is used as a fuel, primarily in the form...Ch. 2 - Prob. 132QRTCh. 2 - Hemoglobin is an iron-containing protein (molar...Ch. 2 - There are three naturally occurring isotopes of...Ch. 2 - Prob. 135QRTCh. 2 - Prob. 136QRTCh. 2 - Prob. 137QRTCh. 2 - An adult human body contains 6.0 L blood, which...Ch. 2 - Prob. 139QRTCh. 2 - Prob. 140QRTCh. 2 - Prob. 141QRTCh. 2 - The present average concentration (mass percent)...Ch. 2 - Prob. 144QRTCh. 2 - A 4.22-g mixture of calcium chloride and sodium...Ch. 2 - A certain metal, M, forms two oxides, M2O and MO....Ch. 2 - If you heat Al with an element from Group 6A, an...Ch. 2 - Prob. 2.ACPCh. 2 - The age of the universe is unknown, but some...Ch. 2 - Prob. 2.CCPCh. 2 - Prob. 2.DCPCh. 2 - Prob. 2.ECP
Knowledge Booster
Similar questions
- Synthesis of ZybanⓇ: 1. Write a mechanism for the bromination of m-chloropropiophenone. Br₂ CH2Cl2 Cl Br 2. Give the expected m/z (to a round number) for the molecular ion from the product above (including isotopic peaks). 3. What signals appeared/disappeared/shifted that indicate that you have your intended product and not starting material? What other impurities are present in your product and how do you know?arrow_forwardSynthesis of Ibuprofen-Part 2: 1. Some pain relievers including ibuprofen (MotrinⓇ) and naproxen (Aleve®) are "α-arylpropanoic acids." Look up the structure of naproxen (AleveⓇ), another a-arylpropionic acid. Using the same reactions that we used for making ibuprofen, show how to make naproxen from the compound below. Show all intermediates and reagents in your synthesis. Show how you would prepare ibuprofen starting from p-isobutylbenzene rather than p-isobutylacetophenenone. What reaction steps would need to change/add? 3. What signals appeared/disappeared/shifted that indicate that you have your intended product and not starting material? What other impurities are present in your product and how do you know?arrow_forwardAcid Catalyzed Aromatization of Carvone: 1. Starting with the ketone, below, draw a mechanism for the reaction to give the phenol as shown. H2SO4 HO- H₂O 2. Why do we use CDCl instead of CHCl, for acquiring our NMR spectra? 3. Why does it not matter which enantiomer of carvone is used for this reaction? What signals appeared/disappeared/shifted that indicate that you have your intended product and not starting material? What other impurities are present in your product and how do you know?arrow_forward
- Assign this H NMRarrow_forwardPlease complete these blanks need that asaparrow_forwardNitration of Methyl Benzoate: 1. Predict the major product for the reaction below AND provide a mechanism. Include ALL resonance structures for the intermediate. C(CH3)3 NO₂* ? 2. Assuming the stoichiometry is 1:1 for the reaction above, what volume of concentrated nitric acid would be required to mononitrate 0.50 grams of the compound above? What product(s) might you expect if you nitrated phenol instead of methyl benzoate? Explain your reasoning. What signals appeared/disappeared/shifted that indicate that you have your intended product and not starting material? What other impurities are present in your product and how do you know?arrow_forward
- Sodium Borohydride Reduction (continued on the next page): 1. Draw the product of each of the reactions below and give the formula mass to the nearest whole number. ? (1) NaBH (2) acid (1) NaBD4 (2) acid ? 2. In mass spectra, alcohols typically break as shown in equation 8 in chapter 11 (refer to your lab manual). The larger group is generally lost and this gives rise to the base peak in the mass spectrum. For the products of each of the reactions in question # 1, draw the ion corresponding to the base peak for that product and give its mass to charge ratio (m/z). 3. Given the reaction below, calculate how many mg of 1-phenyl-1-butanol that can be produced using 31 mg NaBH4 and an excess of butyrophenone. 4. + NaBH4 OH (after workup with dilute HCI) What signals appeared/disappeared/shifted that indicate that you have your intended product and not starting material? What other impurities are present in your product and how do you know?arrow_forwardAspirin from Wintergreen: 1. In isolating the salicylic acid, why is it important to press out as much of the water as possible? Write a step-by-step mechanism for the esterification of salicylic acid with acetic anhydride catalyzed by concentrated H₂SO4. 3. Calculate the exact monoisotopic mass of aspirin showing your work. What signals appeared/disappeared/shifted that indicate that you have your intended product and not starting material? What other impurities are present in your product and how do you know?arrow_forwardSynthesis of Ibuprofen-Part 1: 1. What characteristic absorption band changes would you expect in the IR spectrum on going from p-isobutylacetophenone to 1-(4-isobutylphenyl)-ethanol and then to 1-(4-isobutylphenyl)-1-choroethane as you did in the experiment today? Give approximate wavenumbers associated with each functional group change. Given that the mechanism of the chlorination reaction today involves formation of a benzylic carbocation, explain why the following rearranged product is not formed. محرم محمد 3. Why do we use dilute HCl for the first step of the reaction today and concentrated HCI for the second step? What signals appeared/disappeared/shifted that indicate that you have your intended product and not starting material? What other impurities are present in your product and how do you know?arrow_forward
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