Stereoselectivity Study guides, Revision notes & Summaries

Ogilvie, Organic Chemistry Mechanistic Patterns, 2nd Edition TEST BANK by Ogilvie, Ackroyd, All Chapters 1 - 20, Complete Newest Version CHAPTER 1 Carbon and Its Compounds 2. CHAPTER 2 Anatomy of an Organic Molecule 3. CHAPTER 3 Molecules in Motion: Conformations by Rotations 4. CHAPTER 4 Stereochemistry: Three-Dimensional Structure in Molecules 5. CHAPTER 5 Organic Reaction Mechanism: Using Curved Arrows to Analyze Reaction Mechanisms 6. CHAPTER 6 Acids and Bases 7. CHAPTER 7 π Bonds...

Reagent = Nucleophile Only - ANSWER1° = Sn2 2° = Sn2 3° = Sn1 + E1 (polar medium necessary) Reagent = Strong Nucleophile & Strong Base - ANSWER1° = Sn2 2° = E2 3° = E2 Reagent = Weak Nucleophile and Weak Base - ANSWER1°/2° = No Reaction 3°/resonance stabilized carbocation = Sn1 + E1 (polar medium necessry Reagent = Base Only - ANSWER1° = E2 or Sn2 (if unhindered and no beta-hydrogen with unhindered base) 2° = E2 3° = E2 Examples of Only Nucleophiles - ANSWERCl⁻, ...

IR Spectra correct answer: -Absorption of radiation causes vibrational excitation of functional groups *making it easy to ID functional groups* *0-5000cm-1* H NMR Spectra correct answer: *0-12ppm* C NMR Spectra correct answer: *0-200ppm* Mass Spec correct answer: -Used to measure the molecular weight (mass) of the compound. Alkyne Reactions correct answer: *1* Alkyne + H2/Pd &C = Alkene *2* Alkyne + H2/Lindlav Cat.= Cis Alkene *3* Alkyne + Li or Na/Liquid NH3= Trans Alkene ...

Chem 210 – Reactions Questions 100% Answered!! Reagent = Nucleophile Only - ANSWER1° = Sn2 2° = Sn2 3° = Sn1 + E1 (polar medium necessary) Reagent = Strong Nucleophile & Strong Base - ANSWER1° = Sn2 2° = E2 3° = E2 Reagent = Weak Nucleophile and Weak Base - ANSWER1°/2° = No Reaction 3°/resonance stabilized carbocation = Sn1 + E1 (polar medium necessry Reagent = Base Only - ANSWER1° = E2 or Sn2 (if unhindered and no beta-hydrogen with unhindered base) 2° = E2 3° = E...

Reagent = Nucleophile Only - ANSWER1° = Sn2 2° = Sn2 3° = Sn1 + E1 (polar medium necessary) Reagent = Strong Nucleophile & Strong Base - ANSWER1° = Sn2 2° = E2 3° = E2 Reagent = Weak Nucleophile and Weak Base - ANSWER1°/2° = No Reaction 3°/resonance stabilized carbocation = Sn1 + E1 (polar medium necessry Reagent = Base Only - ANSWER1° = E2 or Sn2 (if unhindered and no beta-hydrogen with unhindered base) 2° = E2 3° = E2 Examples of Only Nucleophiles - ANSWERCl⁻, ...

Bronsted-Lowry Acid Must Have a Proton (H) Bronsted-Lowry Base Must have Lone Pairs or Pi Bonds Neutralization Strong Acid donates a proton to the Strong Base to generate Water and the Conjugate Base Electrophile Electron Loving An atom that wants electrons. An atom that is electron rich. Must have a partial positive charge. (Cation) Nucleophile Nucleus Loving If opposites attract, then a _________ is electron rich. Must have a partial negative charge. (An...

Chapters 12 and 13 wrap up the Organic Chemistry 1 class. We begin Chapter 12 to learn about alcohols and phenols. Students should already have extensive knowledge about alkanes, alkenes and alkynes. They will then learn how the IUPAC name for alcohols differs slightly. They will also learn about oxidation and reduction reactions and how to recognize one. Additionally, students will learn about Grignard reagents and how they contribute to oxidation and reduction reactions. It is also important f...

This is a comprehensive summary that includes both notions and slides of the course, taught by Prof. U. Hennecke at 2nd Ma chemistry students. The reaction mechanisms are extensively covered with a specific focus on the transition states responsible for the induced stereoselectivity.

Prescription writing: required pt and prescriber info - ANSWER-Patient's name and full address Date of prescription Prescriber's full name, address, and phone number Prescriber's DEA # if controlled substance Prescription writing: required drug info - ANSWER-Name (don't abbreviate) Strength and vehicle Dosage Route of administration Directions (Sig) for taking the med: frequency, timing, details specific to drug Amount to be dispensed Refills Critical Rx Information? - ANSWER-...

These notes explain stereosynthesis (stereoselectivity and stereospecificity) and there are practice questions with answers as well.