Chemistry For Today: General, Organic, And Biochemistry, Loose-leaf Version
Chemistry For Today: General, Organic, And Biochemistry, Loose-leaf Version
9th Edition
ISBN: 9781305968707
Author: Spencer L. Seager
Publisher: Brooks Cole
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Chapter 12, Problem 12.75E
Interpretation Introduction

Interpretation:

The number of ethylene monomers (CH2=CH2) contained in a molecule of the polyethylene polymer is to be predicted.

Concept Introduction:

The process by which respective monomers combine to form polymers is known as polymerization. The polymers can be prepared by addition and condensation reactions. The common examples of polymers are polyethene, Teflon, bakelite etc.

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5. Use the MS data to answer the questions on the next page. 14.0 1.4 15.0 8.1 100- MS-IW-5644 26.0 2.8 27.0 6.7 28.0 1.8 29.0 80 4.4 38.0 1.0 39.0 1.5 41.0 1.2 42.0 11.2 43.0 100.0 44.0 4.3 79.0 1.9 80.0 2.6 Relative Intensity 40 81.0 1.9 82.0 2.5 93.0 8.7 20- 95.0 8.2 121.0 2.0 123.0 2.0 136.0 11.8 0 138.0 11.5 20 40 8. 60 a. Br - 0 80 100 120 140 160 180 200 220 m/z Identify the m/z of the base peak and molecular ion. 2 b. Draw structures for each of the following fragments (include electrons and charges): 43.0, 93.0, 95.0, 136.0, and 138.0 m/z. C. Draw a reasonable a-fragmentation mechanism for the fragmentation of the molecular ion to fragment 43.0 m/z. Be sure to include all electrons and formal charges. 6. Using the values provided in Appendix E of your lab manual, calculate the monoisotopic mass for the pyridinium ion (CsH6N) and show your work.
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Stereochemistry: Three possible answers- diastereomers, enantiomers OH CH₂OH I -c=0 21108 1101 41745 HOR CH₂OH IL Но CH₂OH TIL a. Compounds I and III have this relationship with each other: enantiomers b. Compounds II and IV have this relationship with each other: c. Compounds I and II have this relationship with each other: d. *Draw one structure that is a stereoisomer of II, but neither a diastereomer nor an enantiomer. (more than one correct answer)

Chapter 12 Solutions

Chemistry For Today: General, Organic, And Biochemistry, Loose-leaf Version

Ch. 12 - Prob. 12.11ECh. 12 - Prob. 12.12ECh. 12 - What type of hybridized orbital is present on...Ch. 12 - What type of orbital overlaps to form a pi bond in...Ch. 12 - Prob. 12.15ECh. 12 - Explain the difference between geometric and...Ch. 12 - Draw structural formulas and give IUPAC names for...Ch. 12 - Prob. 12.18ECh. 12 - Which of the following alkenes can exist as...Ch. 12 - Draw structural formulas for the following:...Ch. 12 - Prob. 12.21ECh. 12 - In what ways are the physical properties of...Ch. 12 - Prob. 12.23ECh. 12 - Prob. 12.24ECh. 12 - Complete the following reactions. Where more than...Ch. 12 - Prob. 12.26ECh. 12 - Prob. 12.27ECh. 12 - What reagents would you use to prepare each of the...Ch. 12 - What is an important commercial application of...Ch. 12 - Prob. 12.30ECh. 12 - Terpin hydrate is used medicinally as an...Ch. 12 - Prob. 12.32ECh. 12 - Prob. 12.33ECh. 12 - Prob. 12.34ECh. 12 - Prob. 12.35ECh. 12 - Much of todays plumbing in newly built homes is...Ch. 12 - Prob. 12.37ECh. 12 - What type of hybridized orbital is present on...Ch. 12 - How many sigma bonds and how many pi bonds make up...Ch. 12 - Prob. 12.40ECh. 12 - Explain why geometric isomerism is not possible in...Ch. 12 - Give the common name and major uses of the...Ch. 12 - Describe the physical and chemical properties of...Ch. 12 - Prob. 12.44ECh. 12 - Prob. 12.45ECh. 12 - Prob. 12.46ECh. 12 - Prob. 12.47ECh. 12 - Prob. 12.48ECh. 12 - Limonene, which is present in citrus peelings, has...Ch. 12 - A disubstituted cycloalkane such as a exhibits...Ch. 12 - Prob. 12.51ECh. 12 - Prob. 12.52ECh. 12 - Give an IUPAC name for the following as...Ch. 12 - Give an IUPAC name for the following as...Ch. 12 - Name the following compounds, using the prefixed...Ch. 12 - Name the following compounds, using the prefixed...Ch. 12 - Name the following by numbering the benzene ring....Ch. 12 - Name the following by numbering the benzene ring....Ch. 12 - Prob. 12.59ECh. 12 - Write structural formulas for the following:...Ch. 12 - Prob. 12.61ECh. 12 - Prob. 12.62ECh. 12 - Prob. 12.63ECh. 12 - Prob. 12.64ECh. 12 - Prob. 12.65ECh. 12 - Prob. 12.66ECh. 12 - Prob. 12.67ECh. 12 - Prob. 12.68ECh. 12 - Prob. 12.69ECh. 12 - Prob. 12.70ECh. 12 - Prob. 12.71ECh. 12 - Prob. 12.72ECh. 12 - Prob. 12.73ECh. 12 - Prob. 12.74ECh. 12 - Prob. 12.75ECh. 12 - Prob. 12.76ECh. 12 - Prob. 12.77ECh. 12 - Prob. 12.78ECh. 12 - Prob. 12.79ECh. 12 - Prob. 12.80ECh. 12 - Prob. 12.81ECh. 12 - Prob. 12.82ECh. 12 - Prob. 12.83ECh. 12 - The compound CH2=CHCH2CH2CH3 is an example of: a....Ch. 12 - The correct structural for ethyne is: a. HC=CH b....Ch. 12 - Prob. 12.86E
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