For each of the compounds below:A)a) Circle the chromophoreb) State the base value to be used for that moleculec) State the number of additional p bondsd) State the number of "auxochromic" groupse) State the number of "exocyclic" π bondsf) Determine the estimated Amax value for the compoundB)འཚེ་༽C)D)CI

Answered: For each of the compounds below: A) a)…

Chemistry

10th Edition

ISBN:9781305957404

Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Publisher:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Chapter1: Chemical Foundations

Section: Chapter Questions

Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...

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18. draw the mirror image or the compound shown, then determine whether the compound is chiral or achiral. For each structure containing a six-membered ring, consider a single chair conformer
1
I have the following data from an NMR scan. Five peaks; a doublet at about 0.8ppm (6H) a small single septet at about 1.5 ppm (1H), a triplet at 1.6 ppm (2H(, a singlet at about 2.1 ppm (3H), a triplet at about 4.4 ppm (2H). The molecular formula is C7H14O2. I calculated a degree of unsaturation of 1. I have tentatively identified the compound as methyl-4-methylbutanoate. I would appreciate any comments you care to make. Thank you.
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10. Determine the structures of each compound with the given information. A) CsH12 2.0 1.2 1.8 LEO 40 1.5 160 30 140 1.4 1.20 1.2 100 20 B) C4H6O4 IR Data (format= shape of peak, intensity of peak): 3420 cm' (broad, med.), 2932 cm (broad, strong), 1695 cm (narrow, strong), 1419 cm¹ (narrow, med.), 1311 cm (narrow, med.), 1203 cm' (narrow, strong), and a few other weak peaks between 924- 638 cm¹. 1.0 BO Mu 0.8 10 1 0.5 Soivent 0 www.qq.cong 20
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CHEM-240-x1-x2- X 09 KEY Stereoche X *Organic Chemist x functional groups X 08 KEY Constitutic X *Molecular Model X b Draw the lowest Course: NEUR-35 X A https://moodle.viterbo.edu/pluginfile.php/1286283/mod_resource/content/0/Molecular%20Models%20Lab%20assignment%202.. Not syncing A) Read aloud 7 Draw E Highlight O Erase 3 of 4 5. Draw (15,3R)-1-bromo-3-methylcyclohexane in its lowest energy conformation. 6. а. Draw the following molecule as a flat ring skeletal structure with correct stereochemistry. H b. Is the chair in 6a. in its lowest energy conformation? Provide your rationale. 11:31 AM O Type here to search 9. 10/5/2020 +
Answer the following, please provide readable and well explained answers. -Do H-H have IR absorbance peak ? If , at what wavenumber region ? -Do CH2=CH2 have IR absorbance peak ? If, at what wavenumber region ? -Do CH3CH=CH2 have IR absorbance peak ? If, at what wavenumber region ? -Do (CH3)2C=C(CH3)2 have IR absorbance peak ? If, at what wavenumber region ?
PLEASE be CLEAR with how I have to draw the structure. Please draw it CLEARLY. Thanks

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