…Hamlin, Marcel Swart, F. Matthias Bickelhaupt ChemPhysChem 2018, 19 (11), 1315-1330 DOI: 1002/cphc.201701363 A more recent paper computationally examining the effects of various variables on SN2 reaction energetics. Solvolytic Displacement…
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…can then make hypotheses, and test them. The hypotheses that survive experimental testing eventually become known as “laws”, although they are really just very strong theories that have not been…
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…recent offering of massively open online courses (MOOC’s) in the fall. If the type of thinking required for solving the types of problems encountered in organic chemistry can be taught…
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…question when understanding a new reaction: where are the electrons in our starting materials? 2. The Two Reactive Partners In A Substitution Reaction Are An Electron-Rich “Nucleophile” And An Electron-Poor…
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…difficult organic chemistry is. I let myself get taken in by the horror stories around the first exam and did substantially worse on the first exam than I should have…
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…are three examples of nucleophilic substitution reactions. What’s the pattern? In each case, we’re breaking a bond at carbon, and forming a new bond at carbon. (and yes, salts form…
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…so they end up being common exam problems. See if you can draw the key curved arrow to show the rearrangement in this cyclic example: Click to Flip Here’s another…
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…The Mechanism Of Alkyl Shift Reactions Example of An SN1 With Alkyl Shift Ring-Expansion Reactions Also Involve Alkyl Shifts Notes 1. Alkyl Shifts Can Lead To More Stable Carbocations, Too…
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…it does! 4. Examples Of The E1cB Mechanism In Introductory Organic Chemistry: The Aldol Condensation Probably the most commonly encountered example of the E1cB mechanism in introductory organic chemistry is…
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Elimination Reactions (E1) That Occur With Rearrangements – Hydride Or Alkyl Shifts Where there are carbocations (see last post), rearrangement reactions are never far behind. Our old friends have come…
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