Organic Chemistry Roberts & Company Publishers presented by Sapling Learning Mar

Question

Organic Chemistry Roberts & Company Publishers presented by Sapling Learning Marc Loudon (a) An optically inactive compound A (C6H10O4) can be (b) Give the structure for an isomer of Compound A that has a melting resolved into enantiomers and has the following NMR point that is appreciably different spectra: from that of A yet NMR spectra that C NMR: 13.5, 41.2, 177.9 13 are almost identical to those of A. 1H NMR: 1.13 (6H, d, J 7 Hz); 2.65 (2H, quartet, Use wedge/dash bonds, including J 7 Hz), 9.9 (2H, road s, disappears after D20 shake) for any H on a chirality center. Draw either enantiomer, use wedge/dash bonds, including for any H on a chirality center.

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Organic Chemistry Roberts & Company Publishers presented by Sapling Learning Mar

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