CHEMISTRY
2nd Edition
ISBN: 9781593995782
Author: OpenStax
Publisher: XANEDU PUBLISHING
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Textbook Question
Chapter 20, Problem 38E
Write two complete balanced equations for each of the following reactions, one using condensed formulas and one using Lewis structures.
(a) propanol is convened to dipropyl ether.
(b) propene is treated with water in dilute acid.
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Chapter 20 Solutions
CHEMISTRY
Ch. 20 - Write the chemical formula and Lewis structure of...Ch. 20 - What is the difference between the hybridization...Ch. 20 - On a microscopic level, how does the reaction of...Ch. 20 - On a microscopic level, how does the reaction of...Ch. 20 - Explain why unbranched alkenes can form geometric...Ch. 20 - Explain why these two molecules are not isomers:Ch. 20 - Explain why these two molecules are not isomers:Ch. 20 - How does the carbon-atom hybridization change when...Ch. 20 - Write the Lewis structure and molecular formula...Ch. 20 - Write the chemical formula, condensed formula, and...
Ch. 20 - Give the complete IUPAC name for each of the...Ch. 20 - Give the complete IUPAC name for each of the...Ch. 20 - Butane is used as a fuel in disposable lighters....Ch. 20 - Write Lewis structures and name the five...Ch. 20 - Write Lewis structures for the Cis -trans isomers...Ch. 20 - Write structures for the three isomers of the...Ch. 20 - Isooctane is the common name of the isomer of...Ch. 20 - Write Lewis structures and IUPAC names for the...Ch. 20 - Write Lewis structures and IUPAC names for all...Ch. 20 - Name and write the structures of all isomers of...Ch. 20 - Write the structures for all the isomers of the...Ch. 20 - Write Lewis structures and describe the molecular...Ch. 20 - Benzene is one of the compounds used as an octane...Ch. 20 - Teflon is prepared by the polymerization of...Ch. 20 - Write two complete, balanced equations for each of...Ch. 20 - Write two complete, balanced equations for each of...Ch. 20 - What mass of 2-bromopropane could be prepared from...Ch. 20 - Acetylene is a very weak acid; however, it will...Ch. 20 - Ethylene can be produced by the pyrolysis of...Ch. 20 - Why do the compounds hexane, hexanol, and hexane...Ch. 20 - Write condensed formulas and provide IUPAC names...Ch. 20 - Give the complete IUPAC name for each of the...Ch. 20 - Give the complete IUPAC name and the common name...Ch. 20 - Write the condensed structures of both isomers...Ch. 20 - Write the condensed structures of all isomers with...Ch. 20 - Draw the condensed formulas for each of the...Ch. 20 - MTBE, Methyl tert -butyl ether, CH3OC(CH3)3, is...Ch. 20 - Write two complete balanced equations for each of...Ch. 20 - Write two complete balanced equations for each of...Ch. 20 - Order the following molecules from least to most...Ch. 20 - Predict the products of oxidizing the molecules...Ch. 20 - Predict the products of reducing the following...Ch. 20 - Explain why it is not possible to possible a...Ch. 20 - How does hybridization of the substituted carbon...Ch. 20 - Fatty acids are carboxylic acids that have long...Ch. 20 - Write a condensed structural formula, such as...Ch. 20 - Write a condensed structural formula, such as...Ch. 20 - The foul odor of rancid butter is caused by...Ch. 20 - Write the two-resonance structures for the acetate...Ch. 20 - Write two complete, balanced equations for each of...Ch. 20 - Write two complete balanced equations for each of...Ch. 20 - Yields in organic reactions are sometimes low....Ch. 20 - Alcohols A, B and C all have the composition C4H...Ch. 20 - Write the Lewis structures of both isomers with...Ch. 20 - What is the molecular structure about the nitrogen...Ch. 20 - Write the two resonance structures for the...Ch. 20 - Draw Lewis structures for pyridine and its...Ch. 20 - Write the Lewis structures of all isomers with the...Ch. 20 - Write two complete balanced equations for the...Ch. 20 - Write two complete, balanced equations for each of...Ch. 20 - Identify any carbon atoms that change...Ch. 20 - Identify any carbon atoms that change...Ch. 20 - Identify any carbon atoms that change...
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- Use the References to access important values if needed for this question. What is the IUPAC name of each of the the following? 0 CH3CHCNH₂ CH3 CH3CHCNHCH2CH3 CH3arrow_forwardYou have now performed a liquid-liquid extraction protocol in Experiment 4. In doing so, you manipulated and exploited the acid-base chemistry of one or more of the compounds in your mixture to facilitate their separation into different phases. The key to understanding how liquid- liquid extractions work is by knowing which layer a compound is in, and in what protonation state. The following liquid-liquid extraction is different from the one you performed in Experiment 4, but it uses the same type of logic. Your task is to show how to separate apart Compound A and Compound B. . Complete the following flowchart of a liquid-liquid extraction. Handwritten work is encouraged. • Draw by hand (neatly) only the appropriate organic compound(s) in the boxes. . Specify the reagent(s)/chemicals (name is fine) and concentration as required in Boxes 4 and 5. • Box 7a requires the solvent (name is fine). • Box 7b requires one inorganic compound. • You can neatly complete this assignment by hand and…arrow_forwardb) Elucidate compound D w) mt at 170 nd shows c-1 stretch at 550cm;' The compound has the ff electronic transitions: 0%o* and no a* 1H NMR Spectrum (CDCl3, 400 MHz) 3.5 3.0 2.5 2.0 1.5 1.0 0.5 ppm 13C{H} NMR Spectrum (CDCl3, 100 MHz) Solvent 80 70 60 50 40 30 20 10 0 ppm ppm ¹H-13C me-HSQC Spectrum ppm (CDCl3, 400 MHz) 5 ¹H-¹H COSY Spectrum (CDCl3, 400 MHz) 0.5 10 3.5 3.0 2.5 2.0 1.5 1.0 10 15 20 20 25 30 30 -35 -1.0 1.5 -2.0 -2.5 3.0 -3.5 0.5 ppm 3.5 3.0 2.5 2.0 1.5 1.0 0.5 ppmarrow_forward
- Part I. a) Elucidate the structure of compound A using the following information. • mass spectrum: m+ = 102, m/2=57 312=29 • IR spectrum: 1002.5 % TRANSMITTANCE Ngg 50 40 30 20 90 80 70 60 MICRONS 5 8 9 10 12 13 14 15 16 19 1740 cm M 10 0 4000 3600 3200 2800 2400 2000 1800 1600 13 • CNMR 'H -NMR Peak 8 ppm (H) Integration multiplicity a 1.5 (3H) triplet b 1.3 1.5 (3H) triplet C 2.3 1 (2H) quartet d 4.1 1 (2H) quartet & ppm (c) 10 15 28 60 177 (C=0) b) Elucidate the structure of compound B using the following information 13C/DEPT NMR 150.9 MHz IIL 1400 WAVENUMBERS (CM-1) DEPT-90 DEPT-135 85 80 75 70 65 60 55 50 45 40 35 30 25 20 ppm 1200 1000 800 600 400arrow_forward• Part II. a) Elucidate The structure of compound c w/ molecular formula C10 11202 and the following data below: • IR spectra % TRANSMITTANCE 1002.5 90 80 70 60 50 40 30 20 10 0 4000 3600 3200 2800 2400 2000 1800 1600 • Information from 'HAMR MICRONS 8 9 10 11 14 15 16 19 25 1400 WAVENUMBERS (CM-1) 1200 1000 800 600 400 peak 8 ppm Integration multiplicity a 2.1 1.5 (3H) Singlet b 3.6 1 (2H) singlet с 3.8 1.5 (3H) Singlet d 6.8 1(2H) doublet 7.1 1(2H) doublet Information from 13C-nmR Normal carbon 29ppm Dept 135 Dept -90 + NO peak NO peak 50 ppm 55 ppm + NO peak 114 ppm t 126 ppm No peak NO peak 130 ppm t + 159 ppm No peak NO peak 207 ppm по реак NO peakarrow_forwardCould you redraw these and also explain how to solve them for me pleasarrow_forward
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