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Organic Chemistry Hornback 2nd Edition
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Hornback Ch17 671-738
NITRATION OF BENZENE. The OH Of The Nitric Acid Is Protonated In The First Step. The NO 2 + Electrophile Reacts With The Benzene In The Same Manner As Outlined In Figure 17.1. Some Base In The Reaction Mixture, Such As Water, Removes A Proton From The Arenium Ion To Regenerate The Aromatic Ring. Water Then Acts As A Leaving Group 10th, 2024

Hornback Ch07 219-256
A Fischer Projection Results In Inversion Of Configuration At The Chirality Center. Thus, In-terchanging The H And OH On The Lower Chirality Center Of Meso-tartaric Acid Inverts The Configuration At That Chirality Center, Resulting In The (2R,3R)-stereoisomer, ( )-tartaric Acid. 16th, 2024

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Hornback Ch19 803-857
As Was The Case For Nucleophilic Additions To Aldehydes And Ketones, Two Mechanisms Occur For The Reactions In This Chapter: One Under Basic Conditions And One Under Acidic Conditions. Both Of These Start In The Same Manner As The Addition Reaction Mechanisms 29th, 2024

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