Chemistry: Principles and Practice
3rd Edition
ISBN: 9780534420123
Author: Daniel L. Reger, Scott R. Goode, David W. Ball, Edward Mercer
Publisher: Cengage Learning
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Chapter 11, Problem 11.87QE
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Design experiments in UV-Vis to figure the optimal mole ratio of copper (1:1, 2:1, 3:1 and etc)versus ethambutol using all necessary chemicals including dihydrochloride and copper nitrate hemipentahydrate and sodium hydroxide. Show how UV-Vis absorbance and maximum wavelength would change in response
Correct each molecule in the drawing area below so that it has the condensed structure it would have if it were dissolv
a 0.1 M aqueous solution of HCI.
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HO—CH,—C—CH,—OH
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HO–CH,—CH,—C—CH,—OH
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Make the calculations to prepare 2M H2SO4, from concentrated H2SO4 (98%; density: 1.84 g/mL).
Chapter 11 Solutions
Chemistry: Principles and Practice
Ch. 11 - Prob. 11.1QECh. 11 - Prob. 11.2QECh. 11 - Prob. 11.3QECh. 11 - Prob. 11.4QECh. 11 - Prob. 11.5QECh. 11 - Why does a perspiring body achieve greater cooling...Ch. 11 - Prob. 11.7QECh. 11 - Prob. 11.8QECh. 11 - Prob. 11.9QECh. 11 - Prob. 11.10QE
Ch. 11 - Prob. 11.11QECh. 11 - Prob. 11.12QECh. 11 - Prob. 11.13QECh. 11 - Prob. 11.14QECh. 11 - Prob. 11.15QECh. 11 - Prob. 11.16QECh. 11 - Prob. 11.17QECh. 11 - Prob. 11.18QECh. 11 - Prob. 11.19QECh. 11 - Prob. 11.20QECh. 11 - The compounds ethanol (C2H5OH) and dimethyl ether...Ch. 11 - Prob. 11.22QECh. 11 - Prob. 11.23QECh. 11 - An amorphous solid can sometimes be converted to a...Ch. 11 - Prob. 11.25QECh. 11 - Prob. 11.26QECh. 11 - Prob. 11.27QECh. 11 - Prob. 11.28QECh. 11 - Prob. 11.29QECh. 11 - Prob. 11.30QECh. 11 - Prob. 11.31QECh. 11 - Prob. 11.32QECh. 11 - Prob. 11.33QECh. 11 - Prob. 11.34QECh. 11 - Prob. 11.35QECh. 11 - Prob. 11.36QECh. 11 - Prob. 11.37QECh. 11 - Prob. 11.38QECh. 11 - What is the enthalpy change when a 1.00-kg block...Ch. 11 - Prob. 11.40QECh. 11 - Prob. 11.41QECh. 11 - Prob. 11.42QECh. 11 - Prob. 11.43QECh. 11 - Prob. 11.44QECh. 11 - Prob. 11.45QECh. 11 - Prob. 11.46QECh. 11 - Prob. 11.47QECh. 11 - Prob. 11.48QECh. 11 - Identify the kinds of intermolecular forces...Ch. 11 - Prob. 11.50QECh. 11 - Prob. 11.51QECh. 11 - Prob. 11.52QECh. 11 - Prob. 11.53QECh. 11 - Prob. 11.54QECh. 11 - Prob. 11.55QECh. 11 - Prob. 11.56QECh. 11 - Prob. 11.57QECh. 11 - Prob. 11.58QECh. 11 - Prob. 11.59QECh. 11 - Identify the kinds of forces that are most...Ch. 11 - Arrange the following substances in order of...Ch. 11 - Arrange the following substances in order of...Ch. 11 - Prob. 11.63QECh. 11 - Silicon carbide, SiC, is a very hard, high-melting...Ch. 11 - Prob. 11.65QECh. 11 - Calcium oxide consists of a face-centered cubic...Ch. 11 - Prob. 11.67QECh. 11 - Prob. 11.68QECh. 11 - Prob. 11.69QECh. 11 - Prob. 11.70QECh. 11 - Prob. 11.71QECh. 11 - Prob. 11.72QECh. 11 - Prob. 11.73QECh. 11 - Prob. 11.74QECh. 11 - Lithium hydride (LiH) has the sodium chloride...Ch. 11 - Cesium iodide crystallizes as a simple cubic array...Ch. 11 - Palladium has a cubic crystal structure in which...Ch. 11 - Prob. 11.78QECh. 11 - Prob. 11.79QECh. 11 - Prob. 11.80QECh. 11 - Prob. 11.81QECh. 11 - Prob. 11.82QECh. 11 - Prob. 11.83QECh. 11 - Prob. 11.84QECh. 11 - Prob. 11.85QECh. 11 - The coordination number of uniformly sized spheres...Ch. 11 - Prob. 11.87QECh. 11 - Prob. 11.88QECh. 11 - Prob. 11.89QECh. 11 - Prob. 11.90QECh. 11 - Prob. 11.91QECh. 11 - Prob. 11.93QECh. 11 - Prob. 11.94QECh. 11 - A 1.50-g sample of methanol (CH3OH) is placed in...Ch. 11 - Prob. 11.96QECh. 11 - Prob. 11.97QECh. 11 - Prob. 11.98QECh. 11 - Prob. 11.99QECh. 11 - Prob. 11.100QECh. 11 - Prob. 11.103QE
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- H CH3 CH3 b) Write the products of your compound and the following reagents. If the reaction would not work for your compound, write "no reaction" and explain the problem. NaCN H* H₂NNHCH5 H* -à NaBH -à CH2MgBr Cro₁₂ --à H3O+ -à c) Would your compound give a positive Tollen's test? Why or why not?arrow_forwardHomework 4 Chem 204 Dr. Hellwig Consider this compound, which will be referred to as "your compound". a) Name your compound according to the IUPAC system. Include stereochemistry (E/Z/R/S) H CH3 CH3arrow_forwardWhat is the mechanism for this?arrow_forward
- 21.50 Determine the combinations of haloalkane(s) and alkoxide(s) that could be used to synthesize the following ethers through Williamson ether synthesis. (a) (c) (d) (e) (f) H₂COarrow_forward1. Arrange the following in order of increasing bond energy (lowest bond energy first, highest bond energy last). Provide your rationale. C=C, C-F, C=C, C-N, C-C List the bond order for each example.arrow_forwardWhat is the major enolate formed when treated with LDA? And why that one?arrow_forward
- 4. Calculate the total number of sigma bonds and total number of pi bonds in each of the following compounds. a. HH :D: +1 I H-N-C-C-O-H I H b. HH H Н :N=C-C-C=C-CEC-H :0: total o H-C-H H-C = `C-H I H. 11 H-C = C= CH H total o total π total π 1 Harrow_forwardIn the following reaction, what quantity in moles of CH₃OH are required to give off 4111 kJ of heat? 2 CH₃OH (l) + 3 O₂ (g) → 2 CO₂ (g) + 4 H₂O(g) ∆H° = -1280. kJarrow_forwardIndicate the processes in the dismutation of Cu2O.arrow_forward
- 1. Consider these three reactions as the elementary steps in the mechanism for a chemical reaction. 2600 2400 2200 2000 1800 1600 1400 1200 1000 800 Potential Energy (kJ) 600 400 200 0 -200- -400 -600- -800 (i) Cl₂ (g) + Pt(s) → 2Cl (g) + Pt(s) (ii) Cl (g)+ CO (g) + Pt (s) → CICO (g) + Pt (s) Ea = 1550 kJ Ea = 2240 kJ (iii) Cl (g) + CICO (g) → Cl₂CO (g) Ea = 2350 kJ AH=-950 kJ ΔΗ = 575 ΚΙ AH=-825 kJ a. Draw the potential energy diagram for the reaction. Label the data points for clarity. The potential energy of the reactants is 600 kJ Reaction Progress b. What is the overall chemical equation? c. What is the overall change in enthalpy for the above chemical reaction? d. What is the overall amount of activation energy for the above chemical reaction? e. Which reaction intermediate would be considered a catalyst (if any) and why? f. If you were to add 2700kJ of energy to the reaction (e.g. 2700 kl of heat or electricity), would you be able to make the reaction reverse itself (i.e. have…arrow_forwarddraw the enolate anion and the carbonyl that would be needed to make this product through an aldol addition reaction.arrow_forwardDraw the Michael Adduct and the final product of the Robinson annulation reaction. Ignore inorganic byproducts.arrow_forward
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