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    a compound with molecular formula c3h8o produces a broad signal between 3200 and 3600 cm-1 in its ir spectrum and produces two signals in its 13c nmr spectrum. draw the structure of the compound.

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    A compound with molecular formula C_3H_8O produces a broad signal between 3200 and 3600 cm^

    Answer to: A compound with molecular formula C_3H_8O produces a broad signal between 3200 and 3600 cm^-1 in its IR spectrum and produces two signals in its...

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    A compound with molecular formula C_3H_8O produces a broad signal between 3200 and 3600 cm^-1 in...

    A compound with molecular formula C_3H_8O produces a broad signal between 3200 and 3600 cm^-1 in... Question:

    A compound with molecular formula C

    3 3 H 8 8

    O produces a broad signal between 3200 and 3600 cm

    − 1 −1

    in its IR spectrum and produces two signals in its

    13 13

    C-NMR spectrum. Draw the structure of the compound.

    Infrared and NMR Spectroscopies:

    Infrared spectroscopy (IR) involves the interaction of infrared radiation with matter. Functional groups will behave (vibrate, stretch, flex, wiggle, basically move around) at different ranges on a spectrum based on the type of functional group. This can be used to identify and study chemical substances.

    The width and location of the peak in an IR is indicative of what functional group caused it. Alcohol and carboxylic acid peaks are very broad verses carbonyl peaks which are very narrow and sharp. Substituted benzene rings have peaks that correspond to the substitution pattern (, , , , ) in the fingerprint and overtone regions of the IR.

    In nuclear magnetic resonance spectroscopy (NMR), the hydrogen signals split based on dissimilar hydrogens on adjacent atoms. The magnitude of the peaks (area under the peak) tells us how many hydrogens are being split. The number of adjacent hydrogens determines the splitting. Zero dissimilar adjacent hydrogens gives a singlet, one dissimilar adjacent hydrogen gives a doublet, two dissimilar adjacent hydrogens gives a triplet, and so on and so forth. The shift (or delta or peak location) is based on the number and type of electronegative group(s) present, such as carbonyls, alcohols, esters, halogens, etc. Also, shifts will still occur when the hydrogen(s) is(are) bonded to non-carbon atoms, such as N or O.

    Another type of NMR is

    13 13

    C-NMR where the signals are generated by the carbons in the molecule with similar splitting possibilities as in proton-NMR.

    Answer and Explanation:

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    The molecule has 0 degrees of unsaturation

    2 × 3 − 8 2 = 0 2×3−82=0

    , so no rings, double, or triple bonds exist in the molecule. The broad...

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    A compound with molecular formula C3H8O produces a broad signal between 3200 and 3600 cm1 in its IR spectrum and produces two signals in its 1°C NMR spectrum. Draw the structure of the compound.

    A compound with molecular formula C3H8O produces a broad signal between 3200 and 3600 cm1 in its IR spectrum and produces two signals in its 1°C NMR spectrum. Draw the structure of the compound.

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    Transcribed Image Text:A compound with molecular formula C3H8O produces a broad signal between 3200 and 3600 cm1 in its IR spectrum and produces two signals in its 1°C NMR spectrum. Draw the structure of the compound.

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    A compound with molecular formula C3H8O produces a broad

    A compound with molecular formula C3H8O produces a broad signal between 3200 and 3600 cm-1 in its IR spectrum and produces two signals in its 13C NMR spectrum. Deduce the structure of the compound. Step 1 of 2This exercise informs us that there is an unknown compound (with molecular formula \(\mathrm{C}_{3}

    Textbooks / Chemistry / Organic Chemistry 2 / Chapter 16 / Problem 16.53

    A compound with molecular formula C3H8O produces a broad

    ISBN: 9781118454312 78

    Solution for problem 16.53 Chapter 16

    Organic Chemistry | 2nd Edition

    Get Full Solutions 419 Reviews 14 2 Problem 16.53

    A compound with molecular formula C3H8O produces a broad signal between 3200 and 3600 cm-1 in its IR spectrum and produces two signals in its 13C NMR spectrum. Deduce the structure of the compound.

    Step-by-Step Solution:

    Step 1 of 2

    This exercise informs us that there is an unknown compound (with molecular formula

    C3H8O

    ) which produces a broad signal between 3200 and

    3600 cm−1 in its IR

    spectrum and produces two signals in its

    13C

    NMR spectrum. We're asked to deduce the structure of the compound.

    Step 2 of 2

    Chapter 16, Problem 16.53 is Solved

    View Full Solution

    Textbook: Organic Chemistry

    Edition: 2

    Author: David R. Klein

    ISBN: 9781118454312

    Other solutions

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