MCAT Organic Chemistry Review 2018-2019

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6.2 Nucleophilic Addition Reactions


LEARNING GOALS


After   Chapter 6.2,    you will    be  able    to:

Predict the products    of  reacting    aldehydes   or  ketones with    alcohols,   in  the presence    or
absence of acidic conditions
Recall the functional group formed when nitrogen-containing derivatives react with
aldehydes or ketones
Predict the product of the reaction of HCN with aldehydes or ketones, including the
reactivity of the product:

In each of the following reactions, the general reaction mechanism is the same: nucleophilic
addition to a carbonyl. This is one of the most important reaction mechanisms on the MCAT, and
many of the reactions of aldehydes, ketones, and more complex molecules share this general
reaction mechanism. Rather than memorizing each reaction individually, focus on the overall
pattern—then learn how a particular reaction exemplifies it.


MCAT EXPERTISE


Memorizing  one reaction    may help    you to  get one question    right   on  the MCAT,   but
understanding trends and overarching concepts will allow you to answer many more
questions correctly. You will see that the carbonyl carbon is a great target for nucleophilic
attack in many of the reactions in this chapter.
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