Chemistry (OER)
2nd Edition
ISBN: 9781947172616
Author: OpenStax
Publisher: OpenStax College
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Chapter 8, Problem 47E
What charge would be needed on
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For a condensed binary system in equilibrium at constant pressure, indicate the maximum number of phases that can exist.
Part V. Label ad match the carbons in compounds Jane and Diane
w/ the corresponding peak no.
in the
Spectra (Note: use the given peak no. To label the carbons, other peak
no are intentionally
omitted)
7 4 2
-0.13
-0.12
-0.11
-0.10
-0.08
8
CI
Jane
1
-0.09
5
210
200
190
180
170
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120
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100
-8
90
f1 (ppm)
11
8
172.4
172.0
f1 (ppr
HO
CI
NH
Diane
7
3
11
80
80
-80
-R
70
60
60
2
5
-8
50
40
8.
170
160
150
140
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90
-0
80
70
20
f1 (ppm)
15
30
-20
20
-60
60
-0.07
-0.06
-0.05
-0.04
-0.03
-0.02
-0.01
-0.00
-0.01
10
-0.17
16
15
56
16
-0.16
-0.15
-0.14
-0.13
-0.12
-0.11
-0.10
-0.09
-0.08
-0.07
-0.06
-0.05
-0.04
17.8 17.6 17.4 17.2 17.0
f1 (ppm)
-0.03
-0.02
550
106
40
30
20
20
-0.01
-0.00
F-0.01
10
0
Consider the reaction of 2-methylpropane with a halogen. With which halogen will the product be almost exclusively 2-halo-2-methylpropane? 1. F2 2. Cl2 3. Br2 4. I2
Chapter 8 Solutions
Chemistry (OER)
Ch. 8 - Explain how and bonds are similar and how they...Ch. 8 - Draw a curve that describes the energy of a system...Ch. 8 - Explain why bonds occur at specific average bond...Ch. 8 - Use valence bond theory to explain the bonding in...Ch. 8 - Use valence bond theory to explain the bonding in...Ch. 8 - How many and bonds are present in the molecule...Ch. 8 - A friend tells you N2 has three bonds due to...Ch. 8 - Draw the Lewis structures for CO2 and CO, and...Ch. 8 - Why is the concept of hybridization required in...Ch. 8 - Give the shape that describes each hybrid orbital...
Ch. 8 - Explain why a carbon atom cannot form five bonds...Ch. 8 - What is the hybridization of the central atom in...Ch. 8 - A molecule with the formula AB3 could have one of...Ch. 8 - Methionine, CH3SCH2CH2CH(NH2)CO2H, is an amino...Ch. 8 - Sulfuric acid is manufactured by a series of...Ch. 8 - Two important industrial chemicals, ethene, C2H4,...Ch. 8 - For many years after they were discovered, it was...Ch. 8 - Consider nitrous acid, HNO2 (HONO). (a) Write a...Ch. 8 - Strike-anywhere matches contain a layer of KClO3...Ch. 8 - Identify the hybridization of each carbon atom in...Ch. 8 - Write Lewis structures for NF3 and PP5. On the...Ch. 8 - In addition to NF3, two other fluoro derivatives...Ch. 8 - The bond energy of a C—C single bond averages 347...Ch. 8 - For the carbonate ion, CO32, draw all of the...Ch. 8 - A useful solvent that will dissolve salts as well...Ch. 8 - For the molecule allene, H2C=C=CH2, give the...Ch. 8 - Identify the hybridization of the central atom in...Ch. 8 - Describe the molecular geometry and hybridization...Ch. 8 - For each of the following molecules, indicate the...Ch. 8 - For each of the following structures, determine...Ch. 8 - Draw the orbital diagram for carbon in CO2 showing...Ch. 8 - Sketch the distribution of electron density in the...Ch. 8 - How are the following similar, and how do they...Ch. 8 - If molecular orbitals are created by combining...Ch. 8 - Can a molecule with an odd number of electrons...Ch. 8 - Can a molecule with an even number of electrons...Ch. 8 - Why are bonding molecular orbitals lower in energy...Ch. 8 - Calculate the bond order for an ion with this...Ch. 8 - Explain why an electron in the bonding molecular...Ch. 8 - Predict the valence electron molecular orbital...Ch. 8 - Determine the bond order of each member of the...Ch. 8 - For the first ionization energy for an N2...Ch. 8 - Compare the atomic and molecular orbital diagrams...Ch. 8 - Which of the period 2 homonuclear diatomic...Ch. 8 - A friend tells you that the 2s orbital for...Ch. 8 - True or false: Boron contains 2s22p1 valence...Ch. 8 - What charge would be needed on F2 to generate an...Ch. 8 - Predict whether the MO diagram S2 would show s-p...Ch. 8 - Explain why N22+ is diamagnetic, while O24+, which...Ch. 8 - Using the MO diagrams, predict the bond order for...
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- Nonearrow_forwardNonearrow_forwardn Feb 3 A T + 4. (2 pts) Draw the structure of the major component of the Limonene isolated. Explain how you confirmed the structure. 5. (2 pts) Draw the fragment corresponding to the base peak in the Mass spectrum of Limonene. 6. (1 pts) Predict the 1H NMR spectral data of R-Limonene. Proton NMR: 5.3 pon multiplet (H Ringarrow_forward
- Part VI. Ca H 10 O is the molecular formula of compound Tom and gives the in the table below. Give a possible structure for compound Tom. 13C Signals summarized C1 C2 C3 C4 C5 C6 C7 13C shift (ppm) 23.5 27.0 33.0 35.8 127 162 205 DEPT-90 + DEPT-135 + +arrow_forward2. Using the following data to calculate the value of AvapH o of water at 298K. AvapH o of water at 373K is 40.7 kJ/mol; molar heat capacity of liquid water at constant pressure is 75.2J mol-1 K-1 and molar heat capacity of water vapor at constant pressure is 33.6 J mol-1 K-1.arrow_forwardPart VII. Below are the 'HNMR 13 3 C-NMR, COSY 2D- NMR, and HSQC 20-NMR (Similar with HETCOR but axes are reversed) spectra of an organic compound with molecular formula C6H13 O. Assign chemical shift values to the H and c atoms of the compound. Find the structure. Show complete solutions. Predicted 1H NMR Spectrum ли 4.7 4.6 4.5 4.4 4.3 4.2 4.1 4.0 3.9 3.8 3.7 3.6 3.5 3.4 3.3 3.2 3.1 3.0 2.9 2.8 2.7 2.6 2.5 2.4 2.3 2.2 2.1 2.0 1.9 1.8 1.7 1.6 1.5 1.4 1.3 1.2 1.1 1.0 0.9 0.8 f1 (ppm)arrow_forward
- 3. Draw the expanded structural formula, the condensed structural formula, and the skeletal structural formula for 2-pentene. expanded structure: Condensed structure: Skeletal formula: 4. Draw the expanded structural formula, the condensed structural formula, and the skeletal structural formula for 2-methyl-3-heptene. expanded structure: Condensed structure: Skeletal formula: following structurearrow_forwardPart IV. Propose a plausible Structure w/ the following descriptions: a) A 5-carbon hydrocarbon w/ a single peak in its proton decoupled the DEPT-135 Spectrum shows a negative peak C-NMR spectrum where b) what cyclohexane dione isomer gives the largest no. Of 13C NMR signals? c) C5H120 (5-carbon alcohol) w/ most deshielded carbon absent in any of its DEPT Spectivaarrow_forward13C NMR is good for: a) determining the molecular weight of the compound b) identifying certain functional groups. c) determining the carbon skeleton, for example methyl vs ethyl vs propyl groups d) determining how many different kinds of carbon are in the moleculearrow_forward
- 6 D 2. (1 pt) Limonene can be isolated by performing steam distillation of orange peel. Could you have performed this experiment using hexane instead of water? Explain. 3. (2 pts) Using GCMS results, analyze and discuss the purity of the Limonene obtained from the steam distillation of orange peel.arrow_forwardPart III. Arrange the following carbons (in blue) in order of increasing chemical shift. HO B NH 2 A CIarrow_forward6. Choose the compound that will produce the spectrum below and assign the signals as carbonyl, aryl, or alkyl. 100 ō (ppm) 50 0 7. 200 150 Assign all of the protons on the spectrum below. 8. A B 4 E C 3 ō (ppm) 2 1 0 Choose the compound that will produce the spectrum below and assign the signals to the corresponding protons. OH 6 OH 3 2 1 0 4 ō (ppm)arrow_forward
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