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Chemistry Notes: Differences in SN1 and SN2 Substitution Reactions and Spectroscopy - Prof, Study notes of Organic Chemistry

East Tennessee State University (ETSU)Organic Chemistry

Prof. Sheila W. Armentrout

An in-depth analysis of the differences between sn1 and sn2 substitution reactions, focusing on substrate, leaving group, solvent, and nucleophile. It also covers the mechanisms of these reactions, including e1 and e2, stereochemistry, and various terminologies. Additionally, it discusses the interpretation of ir and mass spectroscopy data for various functional groups.

Typology: Study notes

2009/2010

Uploaded on 12/09/2010

jcodyhall 🇺🇸

3 documents

1 / 5

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Download Chemistry Notes: Differences in SN1 and SN2 Substitution Reactions and Spectroscopy - Prof and more Study notes Organic Chemistry in PDF only on Docsity! Differences Based on SN1 and SN2 Substrate/ Leaving Group/ Nucleophile/Solvent E1 and E2 Stereochemistry for SN2 11.12 KNOW MECHANISMS for SN1 // SN2 // E1 // E2 -OH is not a leaving group without being protonated Tosylate – A very good leaving group p361/p369 Must have 4 carbons to get McLagherty MECHANISMS 11.13 p379 11.17 p386 11.21 p391 E1cb only happens when next to carbonyl Figure 11.20 Compare and Contrast Substrate Leaving group Solvent nucleophile 11.15 p385 C SN2 inverts SN1 rhecemic mixture because carbocation is planar

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