Stereogenic - Study guides, Class notes & Summaries

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Organic Chemistry - Final Exam
  • Organic Chemistry - Final Exam

  • Exam (elaborations) • 7 pages • 2023
  • Organic Chemistry - Final Exam Name the 6 polar aprotic solvents - acetone, acetonitrile, DMSO, DMF, HMPA, THF Name the 5 polar protic solvents - acetic acid, ethanol, formic acid, methanol, water ______ and ______ mechanisms are two step reactions that have _____ intermediates. - SN1; E1; 2 Intermediates each ______ and ______ mechanisms are one step reactions that have _____ intermediates. - SN2; E2; 1 Intermediate each Allylic - resonance stabilized (carbon bonde...
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CH7 Stereochemistry TEST BANK
  • CH7 Stereochemistry TEST BANK

  • Exam (elaborations) • 31 pages • 2024
  • 1. Which of the molecules below are chiral? A. only II B. only III C. I and III D. II and III 2. Which of the molecules below are chiral? A. only I B. I and III C. II and III D. I, II, and III 3. Identify the chiral compound(s) below. A. only II B. II and III C. III and IV D. I, II, and IV 4. Which of the following molecules are chiral? A. only II B. only III C. II and III D. I, II, and III 5. How many stereogenic centers are ...
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ACS Organic Chemistry Exam Study Guide Graded A+
  • ACS Organic Chemistry Exam Study Guide Graded A+

  • Exam (elaborations) • 9 pages • 2024
  • ACS Organic Chemistry Exam Study Guide Graded A+ -al -ol or hydroxy- -one -oic acid -oate -ether or alkoxy- Iodo- or Bromo- etc. -amide Amino- or -amine ️Aldehyde Alcohol Ketone Carboxylic acid Ester Ether Alkyl halides Amide Amine Constitutional Isomer ️A compound with the same atoms but different atoms bonded to each other Stereoisomers ️Molecules with the same atoms differing only in 3D configuration Enantiomers ️Stereoisomers with exactly opposite stereoc...
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Organic Chemistry - Final Exam with Complete Solutions (Rated A+)
  • Organic Chemistry - Final Exam with Complete Solutions (Rated A+)

  • Exam (elaborations) • 8 pages • 2024
  • Available in package deal
  • Name the 6 polar aprotic solvents-ANSWER-acetone, acetonitrile, DMSO, DMF, HMPA, THF Name the 5 polar protic solvents-ANSWER-acetic acid, ethanol, formic acid, methanol, water ______ and ______ mechanisms are two step reactions that have _____ intermediates.-ANSWER-SN1; E1; 2 Intermediates each ______ and ______ mechanisms are one step reactions that have _____ intermediates.-ANSWER-SN2; E2; 1 Intermediate each Allylic-ANSWER-resonance stabilized (carbon bonded directly to a C=C) ...
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Chem 51B Pronin Midterm 1 Practice (Questions + Answers)
  • Chem 51B Pronin Midterm 1 Practice (Questions + Answers)

  • Exam (elaborations) • 9 pages • 2022
  • This document is a practice exam worksheet that will provide practice and understanding for Midterm 1 of Chem 51B. This document goes over relevant and significant concepts and problems that will be included in the exam. Good practice!
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Organic Chemistry - Final Exam Complete Solutions 2023
  • Organic Chemistry - Final Exam Complete Solutions 2023

  • Exam (elaborations) • 6 pages • 2023
  • Organic Chemistry - Final Exam Complete Solutions 2023 Name the 6 polar aprotic solvents acetone, acetonitrile, DMSO, DMF, HMPA, THF Name the 5 polar protic solvents acetic acid, ethanol, formic acid, methanol, water ______ and ______ mechanisms are two step reactions that have _____ intermediates. SN1; E1; 2 Intermediates each ______ and ______ mechanisms are one step reactions that have _____ intermediates. SN2; E2; 1 Intermediate each Allylic resonance stabilized (carbon bonded direct...
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Organic Chemistry I - Chapter 5: Stereochemistry Organic Chemistry I - Chapter 5: Stereochemistry
  • Organic Chemistry I - Chapter 5: Stereochemistry

  • Class notes • 7 pages • 2023
  • Notes were taken from my Orgo class, chapter 5
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STEREOCHEMISTRY
  • STEREOCHEMISTRY

  • Class notes • 7 pages • 2022
  • Overview of different types of stereochemistry. Explains how to name different stereoisomers, differences between, drawing, chirality, stereogenic centers and bonds.
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organic chemistry
  • organic chemistry

  • Class notes • 25 pages • 2022
  • Asymmetric synthesis is a subclass of stereoselective reactions, where a new chiral stereogenic unit is created during a reaction. The new stereogenic unit can be a chiral centre, a chiral axis or a chiral plane. The reaction must proceed with unequal formation of possible stereoisomers. The chiral unit can be produced from substrates bearing pro-chiral units such as pro-chiral centre, a pro-chiral plane or a pro-chiral axis. The pro-chiral unit can be enantiotopic or diastereotopic. Thus, two e...
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