General Chemistry: Atoms First
2nd Edition
ISBN: 9780321809261
Author: John E. McMurry, Robert C. Fay
Publisher: Prentice Hall
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Textbook Question
Chapter 8.3, Problem 8.2P
Calculate the work in kilojoules done during a synthesis of ammonia in which the volume contracts from 8.6 L to 4.3 L at a constant external pressure of 44 atm. In which direction does the work energy flow? What is the sign of the energy change?
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5 (a). Using the peak information you listed in the tables for
both structures, assign each peak to that portion of the
structure that produces the peak in the NMR spectrum. Draw
this diagram on your own sheet of paper and attach the sketch
of your drawing to this question.
Question 6
5 (b). Using the peak information you listed in the tables for
both structures, assign each peak to that portion of the
structure that produces the peak in the NMR spectrum. Draw
this diagram on your own sheet of paper and attach the sketch
of your drawing to this question.
Question 7
6. Are there any differences between the spectra you obtained
in Beyond Labz and the predicted spectra? If so, what were
the differences?
<
2. Predict the NMR spectra for each of these two
compounds by listing, in the NMR tables below, the
chemical shift, the splitting, and the number of
hydrogens associated with each predicted peak. Sort the
peaks from largest chemical shift to lowest.
**Not all slots must be filled**
Peak
Chemical Shift (d)
5.7
1
Multiplicity
multiplate
..........
5.04
double of doublet
2
4.98
double of doublet
3
4.05
doublet of quartet
4
5
LO
3.80
quartet
1.3
doublet
6
Peak
Chemical Shift (d)
Multiplicity
Chapter 8 Solutions
General Chemistry: Atoms First
Ch. 8.2 - Which of the following are state functions, and...Ch. 8.3 - Calculate the work in kilojoules done during a...Ch. 8.3 - How much work is done in kilojoules, and in which...Ch. 8.4 - The following reaction has E = 186 kJ/mol. (a) Is...Ch. 8.5 - Assuming that Coca Cola has the same specific heat...Ch. 8.5 - What is the specific heat of lead if it takes 97.2...Ch. 8.5 - When 25.0 mL of 1.0 M H2SO4 is added to 50.0 mL of...Ch. 8.6 - The reaction between hydrogen and oxygen to yield...Ch. 8.6 - The explosion of 2.00 mol of solid trinitrotoluene...Ch. 8.7 - How much heat in kilojoules is evolved or absorbed...
Ch. 8.7 - Nitromethane (CH3NO2), sometimes used as a fuel in...Ch. 8.8 - The industrial degreasing solvent methylene...Ch. 8.8 - The reaction of A with B to give D proceeds in two...Ch. 8.8 - Draw a Hesss law diagram similar to that in...Ch. 8.9 - Use the information in Table 8.2 to calculate H in...Ch. 8.9 - Use the information in Table 8.2 to calculate H in...Ch. 8.10 - Use the data in Table 8.3 to calculate an...Ch. 8.10 - Use the data in Table 8.3 to calculate an...Ch. 8.11 - Liquid butane (C4H10), the fuel used in many...Ch. 8.12 - Ethane, C2H6, can be prepared by the reaction of...Ch. 8.12 - Is the reaction represented in the following...Ch. 8.12 - Which of the following reactions are spontaneous...Ch. 8.12 - Is the Haber process for the industrial synthesis...Ch. 8.12 - The following reaction is exothermic: (a) Write a...Ch. 8.12 - Write balanced equations for the combustion...Ch. 8.12 - Biodiesel has a more favorable (more negative)...Ch. 8 - The following reaction is exothermic: (a) Write a...Ch. 8 - Imagine a reaction that results in a change in...Ch. 8 - Redraw the following diagram to represent the...Ch. 8 - Prob. 8.30CPCh. 8 - Prob. 8.31CPCh. 8 - A reaction is carried out in a cylinder fitted...Ch. 8 - The following drawing portrays a reaction of the...Ch. 8 - Prob. 8.34CPCh. 8 - The following reaction of A3 molecules is...Ch. 8 - Prob. 8.36SPCh. 8 - What is internal energy?Ch. 8 - Prob. 8.38SPCh. 8 - Assume that the kinetic energy of a 1400 kg car...Ch. 8 - Prob. 8.40SPCh. 8 - The addition of H2 to CC double bonds is an...Ch. 8 - Prob. 8.42SPCh. 8 - Prob. 8.43SPCh. 8 - Prob. 8.44SPCh. 8 - Prob. 8.45SPCh. 8 - Prob. 8.46SPCh. 8 - Does a measurement carried out in a bomb...Ch. 8 - Prob. 8.48SPCh. 8 - Prob. 8.49SPCh. 8 - Prob. 8.50SPCh. 8 - When 0.187 g of benzene, C6H6, is burned in a bomb...Ch. 8 - When a solution containing 8.00 g of NaOH in 50.0...Ch. 8 - Prob. 8.53SPCh. 8 - Prob. 8.54SPCh. 8 - Prob. 8.55SPCh. 8 - Prob. 8.56SPCh. 8 - Prob. 8.57SPCh. 8 - Prob. 8.58SPCh. 8 - Prob. 8.59SPCh. 8 - Prob. 8.60SPCh. 8 - Prob. 8.61SPCh. 8 - Used in welding metals, the reaction of acetylene...Ch. 8 - Prob. 8.63SPCh. 8 - The familiar ether used as an anesthetic agent is...Ch. 8 - How much energy in kilojoules is required to...Ch. 8 - Prob. 8.66SPCh. 8 - Prob. 8.67SPCh. 8 - Prob. 8.68SPCh. 8 - Prob. 8.69SPCh. 8 - Prob. 8.70SPCh. 8 - Prob. 8.71SPCh. 8 - Prob. 8.72SPCh. 8 - Prob. 8.73SPCh. 8 - Prob. 8.74SPCh. 8 - Prob. 8.75SPCh. 8 - Prob. 8.76SPCh. 8 - Prob. 8.77SPCh. 8 - Prob. 8.78SPCh. 8 - Prob. 8.79SPCh. 8 - Prob. 8.80SPCh. 8 - Prob. 8.81SPCh. 8 - Styrene (C8H8), the precursor of polystyrene...Ch. 8 - Prob. 8.83SPCh. 8 - Prob. 8.84SPCh. 8 - Prob. 8.85SPCh. 8 - Prob. 8.86SPCh. 8 - Prob. 8.87SPCh. 8 - Use the bond dissociation energies in Table 8.3 on...Ch. 8 - Use the bond dissociation energies in Table 8.3 to...Ch. 8 - Prob. 8.90SPCh. 8 - Prob. 8.91SPCh. 8 - Prob. 8.92SPCh. 8 - Prob. 8.93SPCh. 8 - Prob. 8.94SPCh. 8 - Prob. 8.95SPCh. 8 - Prob. 8.96SPCh. 8 - Prob. 8.97SPCh. 8 - Prob. 8.98SPCh. 8 - Prob. 8.99SPCh. 8 - Prob. 8.100SPCh. 8 - Prob. 8.101SPCh. 8 - Prob. 8.102SPCh. 8 - Tell whether reactions with the following values...Ch. 8 - Prob. 8.104SPCh. 8 - Prob. 8.105SPCh. 8 - Prob. 8.106SPCh. 8 - Prob. 8.107SPCh. 8 - Prob. 8.108SPCh. 8 - Prob. 8.109SPCh. 8 - When 1.50 g of magnesium metal is allowed to react...Ch. 8 - Use the data in Appendix B to find standard...Ch. 8 - Prob. 8.112CHPCh. 8 - The boiling point of a substance is defined as the...Ch. 8 - What is the melting point of benzene in kelvin if...Ch. 8 - Metallic mercury is obtained by heating the...Ch. 8 - Prob. 8.116CHPCh. 8 - Methanol (CH3OH) is made industrially in two steps...Ch. 8 - Isooctane, C8H18, is the component of gasoline...Ch. 8 - We said in Section 8.1 that the potential energy...Ch. 8 - For a process to be spontaneous, the total entropy...Ch. 8 - Set up a Hesss law cycle, and use the following...Ch. 8 - Prob. 8.122CHPCh. 8 - Prob. 8.123CHPCh. 8 - Prob. 8.124CHPCh. 8 - Citric acid has three dissociable hydrogens. When...Ch. 8 - Prob. 8.126CHPCh. 8 - Imagine that you dissolve 10.0 g of a mixture of...Ch. 8 - Prob. 8.128CHPCh. 8 - Prob. 8.129MPCh. 8 - Phosgene, COCl2(g), is a toxic gas used as an...Ch. 8 - Prob. 8.131MPCh. 8 - (a) Write a balanced equation for the reaction of...Ch. 8 - Prob. 8.133MPCh. 8 - Reaction of gaseous fluorine with compound X...
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- Interpreting NMR spectra is a skill that often requires some amount of practice, which, in turn, necessitates access to a collection of NMR spectra. Beyond Labz Organic Synthesis and Organic Qualitative Analysis have spectral libraries containing over 700 1H NMR spectra. In this assignment, you will take advantage of this by first predicting the NMR spectra for two closely related compounds and then checking your predictions by looking up the actual spectra in the spectra library. After completing this assignment, you may wish to select other compounds for additional practice. 1. Write the IUPAC names for the following two structures: Question 2 Question 3 2. Predict the NMR spectra for each of these two compounds by listing, in the NMR tables below, the chemical shift, the splitting, and the number of hydrogens associated with each predicted peak. Sort the peaks from largest chemical shift to lowest. **Not all slots must be filled**arrow_forward11:14 ... worksheets.beyondlabz.com 3. To check your predictions, click this link for Interpreting NMR Spectra 1. You will see a list of all the - compounds in the spectra library in alphabetical order by IUPAC name. Hovering over a name in the list will show the structure on the chalkboard. The four buttons on the top of the Spectra tab in the tray are used to select the different spectroscopic techniques for the selected compound. Make sure the NMR button has been selected. 4. Scroll through the list of names to find the names for the two compounds you have been given and click on the name to display the NMR spectrum for each. In the NMR tables below, list the chemical shift, the splitting, and the number of hydrogens associated with each peak for each compound. Compare your answers to your predictions. **Not all slots must be filled** Peak Chemical Shift (d) Multiplicity 1 2 3 4 5arrow_forwardО δα HO- H -Br δα HO-- + + -Br [B] 8+ HO- -Br δα नarrow_forward
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