Question 6 of 7 (1 point) | Question Attempt: 1 of 1= 1✓2✓ 3✓ 4✓ 56✓ 7This organic molecule is dissolved in a basic aqueous solution:Jen ✓?A short time later sensitive infrared spectroscopy reveals the presence of a new C-OH stretch absorption. That is,must now be a new molecule present with at least one C- OH bond.there18In the drawing area below, show the detailed mechanism that could convert the molecule above into the new molecule Ar©+Click and drag to startdrawing a structure.Add/Remove stepClick anddrawingSave For LaterSubmit Assignment

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Answered: Question 6 of 7 (1 point) | Question…

Organic Chemistry: A Guided Inquiry

2nd Edition

ISBN:9780618974122

Author:Andrei Straumanis

Publisher:Andrei Straumanis

Chapter8: Addition Via Carbocation

Section: Chapter Questions

Problem 11E

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This organic molecule is dissolved in a basic aqueous solution: A short time later sensitive infrared spectroscopy reveals the presence of a new C-OH stretch absorption. That is, there must now be a new molecule pre with at least one C-OH bond. In the drawing area below, show the detailed mechanism that could convert the molecule above into the new molecule.
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i need to draw an ir spectrum based on the numbers below and label them a b c d e ect...
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The structure shown below has 3 peaks in the ¹H NMR spectrum. Order them from the furthest downfield (left) to furthest upfield (right, toward O). Left (downfield) [Select] [Select] Ан [Select] Ill!!!! H H B H (Illum... |||||| CI с H H middle right (upfield, closer to zero)
How could spectroscopy be used to support that the below reaction occurred? Choose all that apply. excess CH HCI H,C, CH3 v 1st attempt Choose one or more: O Use IR; the product has a strong broad peak at 2200 cm-1, but the starting material does not. O Use UV-vis; the product would not show an absorbance in the spectrum range due to a shorter Åmax from that of the starting material O Use IR; the product has a sharp narrow peak at 3300 cm-1, but the starting material does not. O IR will not be useful as no detectable change in the spectrum will occur. O UV-vis will not be useful because no change in åmax Would occur. Use IR; the starting material has a sharp narrow peak at 3300 cm-1, but the product does not. Use UV-vis; the product would show an absorbance at a longer Âmax from that of the starting material. O Use IR; the starting material has a strong broad peak at 2200 cm-1, but the product does not.
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Hexamethylbenzene undergoes free-radical chlorination to give one monochlorinated product (C12H17Cl) and four dichlorinated products (C12H16Cl2). These products are easily separated by GC-MS, but the dichlorinated products are difficultto distinguish by their mass spectra. Draw the monochlorinated product and the four dichlorinated products, and explainhow 13C NMR would easily distinguish among these compounds
Take a look at the reaction in the first image that give two products A and B The second picture shows the DEPT 90 (TOP) and DEPT 135 (BOTTOM) of the compound that was isolated as only product of this reaction: In both spectra there are 7 signals between 120 and 140 ppm. How can you use these DEPT spectra to establish if product A or product B was formed in this reaction? Explain your reasoning.
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Task 2: Systematically analyze the IR spectra 1-4 presented on the following pages and match them with the structures of compounds indicated below. Label the diagnostic absorptions on the spectra and then complete the table below each spectrum. Note: The number of structures provided below is more than the number of spectra provided. The structures indicated below are constitutional isomers of C4H602. OH HO. HO Но. compound 1 compound 2 compound 3 compound 4 compound 5 compound 6 Spectrum 1: FTIR NEAT 100 90 IN 80 3p93.3 1625.7- 592.9 70 406 9 60 848.5636.4 977.7 1294.0 50 L9507877. 40 1020 30 1646 9 1371.1 20 1137.8 1762.6 1218 8 45 00 42 50 4000 37 50 3500 3250 30 00 27 50 2500 2250 2000 1750 1500 1250 1000 750 500 250 Wavenumbers (cm-1) © 20 18, Sigma-Aldrich Co. ALL RIGHTS RESERVED Bond vibration Expected frequency range (cm-1) (from IR absorption table) Observed absorption (cm-1) Functional group(s): Structure: % Transmittance

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