
Chemistry by OpenStax (2015-05-04)
1st Edition
ISBN: 9781938168390
Author: Klaus Theopold, Richard H Langley, Paul Flowers, William R. Robinson, Mark Blaser
Publisher: OpenStax
expand_more
expand_more
format_list_bulleted
Textbook Question
Chapter 12, Problem 57E
The rate of a certain reaction doubles for every 10 °C rise in temperature.
(a) How much faster does the reaction proceed at 45 °C than at 25 °C?
(b) How much faster does the reaction proceed at 95 °C than at 25 °C?
Expert Solution & Answer

Trending nowThis is a popular solution!

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 12 Solutions
Chemistry by OpenStax (2015-05-04)
Ch. 12 - What is the difference between average rate,...Ch. 12 - Ozone decomposes to oxygen according to the...Ch. 12 - In the nuclear industry, chlorine trifluoride is...Ch. 12 - A study of the rate of dimerization of C4H6 gave...Ch. 12 - A study of the rate of the reaction represented as...Ch. 12 - Consider the following reaction in aqueous...Ch. 12 - Describe the effect of each of the following on...Ch. 12 - Explain why an egg cooks move slowly in boiling...Ch. 12 - Go to the PhET Reactions and change to Angled...Ch. 12 - In the PhET Reactions tab to observe how multiple...
Ch. 12 - In the PhET Reactions under Options. (a) Leave...Ch. 12 - How do the rate of a reaction and its rate...Ch. 12 - Doubling the concentration of a reactant increases...Ch. 12 - Tripling the concentration of a reactant increases...Ch. 12 - How much and in what direction will each of the...Ch. 12 - How will each of the following affect the rate of...Ch. 12 - Regular ?ights of supersonic aircraft in the...Ch. 12 - Radioactive phosphorus is used in the study of...Ch. 12 - The rate constant for the radioactive decay of 14C...Ch. 12 - The decomposition of acetaldehyde is a second...Ch. 12 - Alcohol is removed from the bloodstream by a...Ch. 12 - Under certain conditions the decomposition of...Ch. 12 - Nitrosyl chloride, NOCI, decomposes to NO and CI2....Ch. 12 - From the following data, determine the rate...Ch. 12 - Nitrogen monoxide reacts with chlorine according...Ch. 12 - Hydrogen reacts with nitrogen monoxide to form...Ch. 12 - For the reaction AB+C, the following data were...Ch. 12 - For the reaction QW+X, the following data were...Ch. 12 - The rate constant for the ?rst-order decomposition...Ch. 12 - The annual production of HNO3 in 2013 was 60...Ch. 12 - The following data have been determined for the...Ch. 12 - Describe how graphical methods can be used to...Ch. 12 - Use the data provided to graphically determine the...Ch. 12 - Use the data provided in a graphical method to...Ch. 12 - Pure ozone decomposes slowly to oxygen, 2O33O2(g)....Ch. 12 - From the given data, use a graphical method to...Ch. 12 - What is the half-life for the first-order decay of...Ch. 12 - What is the half-life for the first-order decay of...Ch. 12 - What is the half-life for the decomposition of...Ch. 12 - What is the half-life for the decomposition of O3...Ch. 12 - The reaction of compound A to give compounds C and...Ch. 12 - The half-life of a reaction of compound A to give...Ch. 12 - Some bacteria are resistant to the antibiotic...Ch. 12 - Both technetium-99 and thallium-201 are used to...Ch. 12 - There are two molecules with the formula C3H6...Ch. 12 - Fluorine-18 is a radioactive isotope that decays...Ch. 12 - Suppose that the half-life of steroids taken by an...Ch. 12 - Recently, the skeleton of King Richard III was...Ch. 12 - Nitroglycerine is an extremely sensitive...Ch. 12 - For the past 10 years, the unsaturated hydrocarbon...Ch. 12 - Chemical reactions occur when reactants collide....Ch. 12 - When every collision between reactants leads to a...Ch. 12 - What is the activation energy of a reaction, and...Ch. 12 - Account for the relationship between the rate of a...Ch. 12 - Describe how graphical methods can be used to...Ch. 12 - How does an increase in temperature affect rate of...Ch. 12 - The rate of a certain reaction doubles for every...Ch. 12 - In an experiment, a sample of NaClO3 was 90%...Ch. 12 - The rate constant at 325 C for the decomposition...Ch. 12 - The rate constant for the decomposition of...Ch. 12 - An elevated level of the enzyme alkaline...Ch. 12 - In terms of collision theory, to which of the...Ch. 12 - Hydrogen iodide, HI, decomposes in the gas phase...Ch. 12 - The element Co exists in two oxidation states,...Ch. 12 - The hydrolysis of the sugar sucrose to the sugars...Ch. 12 - Use the PhET Reactions Single collision" tab of...Ch. 12 - Use the PhET Reactions Single collision tab of the...Ch. 12 - Why awe elementary reactions involving three or...Ch. 12 - In general, can we predict the effect of doubling...Ch. 12 - Define these terms: (a) unimolecular reaction (b)...Ch. 12 - What is the rate equation for the elementary...Ch. 12 - Given the following reactions and the...Ch. 12 - Write the rate equation for each of the following...Ch. 12 - Nitrogen (Il) oxide, NO, reacts with hydrogen, H2,...Ch. 12 - Experiments were conducted to study the rate of...Ch. 12 - The reaction of CO with CI2 gives phosgene...Ch. 12 - . Account for the increase in reaction rate...Ch. 12 - Compare the functions of homogeneous and...Ch. 12 - Consider this scenario and answer the following...Ch. 12 - For each of the following pairs of reaction...Ch. 12 - For each of the following pairs of reaction...Ch. 12 - For each of the following reaction diagrams,...Ch. 12 - For each of the following reaction diagrams,...Ch. 12 - Based on the diagrams in Exercise 12.83, which of...Ch. 12 - Based on the diagram in Exercise 12.83, which of...
Additional Science Textbook Solutions
Find more solutions based on key concepts
Choose the element with the larger atoms from each pair. a. Sn or Si b. Br or Ga c. Sn or Bi d. Se or Sn
Introductory Chemistry (6th Edition)
One isomer of methamphetamine is the addictive illegal drug known as crank. Another isomer is a medicine for si...
Campbell Essential Biology (7th Edition)
Endospore formation is called (a) _____. It is initiated by (b) _____. Formation of a new cell from an endospor...
Microbiology: An Introduction
How can 1H NMR distinguish between the compounds in each of the following pairs?
Organic Chemistry (8th Edition)
If someone at the other end of a room smokes a cigarette, you may breathe in some smoke. The movement of smoke ...
Campbell Essential Biology with Physiology (5th Edition)
A source of electromagnetic radiation produces infrared light. Which of the following could be the wavelength ...
Chemistry: The Central Science (14th Edition)
Knowledge Booster
Learn more about
Need a deep-dive on the concept behind this application? Look no further. Learn more about this topic, chemistry and related others by exploring similar questions and additional content below.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
arrow_back_ios
SEE MORE QUESTIONS
arrow_forward_ios
Recommended textbooks for you
- Chemistry: Principles and PracticeChemistryISBN:9780534420123Author:Daniel L. Reger, Scott R. Goode, David W. Ball, Edward MercerPublisher:Cengage LearningChemistry: The Molecular ScienceChemistryISBN:9781285199047Author:John W. Moore, Conrad L. StanitskiPublisher:Cengage LearningChemistry by OpenStax (2015-05-04)ChemistryISBN:9781938168390Author:Klaus Theopold, Richard H Langley, Paul Flowers, William R. Robinson, Mark BlaserPublisher:OpenStax
- ChemistryChemistryISBN:9781305957404Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCostePublisher:Cengage LearningChemistry: An Atoms First ApproachChemistryISBN:9781305079243Author:Steven S. Zumdahl, Susan A. ZumdahlPublisher:Cengage Learning

Chemistry: Principles and Practice
Chemistry
ISBN:9780534420123
Author:Daniel L. Reger, Scott R. Goode, David W. Ball, Edward Mercer
Publisher:Cengage Learning

Chemistry: The Molecular Science
Chemistry
ISBN:9781285199047
Author:John W. Moore, Conrad L. Stanitski
Publisher:Cengage Learning

Chemistry by OpenStax (2015-05-04)
Chemistry
ISBN:9781938168390
Author:Klaus Theopold, Richard H Langley, Paul Flowers, William R. Robinson, Mark Blaser
Publisher:OpenStax

Chemistry
Chemistry
ISBN:9781305957404
Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Publisher:Cengage Learning

Chemistry: An Atoms First Approach
Chemistry
ISBN:9781305079243
Author:Steven S. Zumdahl, Susan A. Zumdahl
Publisher:Cengage Learning

Kinetics: Chemistry's Demolition Derby - Crash Course Chemistry #32; Author: Crash Course;https://www.youtube.com/watch?v=7qOFtL3VEBc;License: Standard YouTube License, CC-BY