Essential Organic Chemistry Study Guide & Solution Manual, Books a la Carte Edition
Essential Organic Chemistry Study Guide & Solution Manual, Books a la Carte Edition
3rd Edition
ISBN: 9780134255644
Author: Bruice, Paula Yurkanis
Publisher: PEARSON
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Chapter 16, Problem 23P
Interpretation Introduction

Interpretation:

The product obtained from the reaction of D-ribose with one equivalent of methanol and HCl is to be predicted.

Concept Introduction:

The hydroxyl group of anomeric carbon is protonated by an acid.  The lone pair on the ring helps in eliminating a molecule of water which results in the formation of oxocarbenium ion.  It is planar molecule.  When the alcohol approaches from the top of the plane, the β-glycoside is formed.  When the alcohol approaches from the bottom of plane, the α-glycoside is formed.

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What spectral features allow you to differentiate the product from the starting material? Use four separate paragraphs for each set of comparisons. You should have one paragraph each devoted to MS, HNMR, CNMR and IR. 2) For MS, the differing masses of molecular ions are a popular starting point. Including a unique fragmentation is important, too. 3) For HNMR, CNMR and IR state the peaks that are different and what makes them different (usually the presence or absence of certain groups). See if you can find two differences (in each set of IR, HNMR and CNMR spectra) due to the presence or absence of a functional group. Include peak locations. Alternatively, you can state a shift of a peak due to a change near a given functional group. Including peak locations for shifted peaks, as well as what these peaks are due to. Ideally, your focus should be on not just identifying the differences but explaining them in terms of functional group changes.
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