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Organic chemistry mechanistic patterns 1st Edition by Ghis William Ogilvie, Nathan Ackroyd, Scott Browning ISBN 017650026X 9780176500269

  • SKU: BELL-21347232
Organic chemistry mechanistic patterns 1st Edition by Ghis William Ogilvie, Nathan Ackroyd, Scott Browning ISBN 017650026X 9780176500269
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Organic chemistry mechanistic patterns 1st Edition by Ghis William Ogilvie, Nathan Ackroyd, Scott Browning ISBN 017650026X 9780176500269 instant download after payment.

Publisher: Nelson College Indigenous; W. Ross MacDonald School Resource Services Library
File Extension: PDF
File size: 234.12 MB
Author: Ackroyd, Nathan; Browning, C. Scott; Deslongchamps, Ghislain; Dryden, Neil; Lee, Felix; Ogilvie, William Walter; Sauer, Effie
ISBN: 9780176500269, 017650026X
Language: English
Year: 2017

Product desciption

Organic chemistry mechanistic patterns 1st Edition by Ghis William Ogilvie, Nathan Ackroyd, Scott Browning ISBN 017650026X 9780176500269 by Ackroyd, Nathan; Browning, C. Scott; Deslongchamps, Ghislain; Dryden, Neil; Lee, Felix; Ogilvie, William Walter; Sauer, Effie 9780176500269, 017650026X instant download after payment.

Organic chemistry mechanistic patterns 1st Edition by Ghis William Ogilvie, Nathan Ackroyd, Scott Browning - Ebook PDF Instant Download/Delivery: 017650026X, 9780176500269
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Product details:

ISBN 10: 017650026X 
ISBN 13: 9780176500269
Author: Ghis William Ogilvie, Nathan Ackroyd, Scott Browning

Organic Mechanistic Patterns is the very first introductory organic chemistry title that holistically focuses on a mechanistic approach; an approach that has proven to achieve a deeper understanding of chemical reactivity. This mechanistic approach to the dynamic world of organic chemistry visualizes reactivity as a collection of patterns in electron movement, making it possible for students to describe why a reaction occurred. Recognizing patterns of electron flow between seemingly different reactions can allow students to predict how a chemical will react, even if they have never seen a particular reaction before. The text takes great care to establish a progression of reactivity, from simple to complex, introducing functional groups as necessary, while focusing on the reaction at hand rather than the various things that each functional group does. Together, we seek to open students’ eyes to the dynamic world of organic chemistry with a more powerful and systematic approach to learning.

Organic chemistry mechanistic patterns 1stTable of contents:

  1. Carbon and Its Compounds

  2. Anatomy of an Organic Molecule

  3. Molecules in Motion: Conformations by Rotations

  4. Stereochemistry: Three-Dimensional Structure in Molecules

  5. Organic Reaction Mechanism: Using Curved Arrows to Analyze Reaction Mechanisms

  6. Acids and Bases

  7. π Bonds as Electrophiles: Reactions of Carbonyls and Related Functional Groups

  8. π Bonds as Nucleophiles: Reactions of Alkenes, Alkynes, Dienes, and Enols

  9. Conjugation and Aromaticity

  10. Synthesis Using Aromatic Materials: Electrophilic Aromatic Substitution and Directed Ortho Metalation

  11. Displacement Reactions on Saturated Carbons: SN1 and SN2 Substitution Reactions

  12. Formation of π Bonds by Elimination Processes: Elimination and Oxidation Reactions

  13. Structure Determination I: Nuclear Magnetic Resonance Spectroscopy

  14. Structure Determination II: Mass Spectrometry and Infrared Spectroscopy

  15. π Bond Electrophiles Connected to Leaving Groups: Carboxylic Acid Derivatives

  16. π Bonds with Hidden Leaving Groups: Reactions of Acetals and Related Compounds

  17. Carbonyl-Based Nucleophiles: Aldol, Claisen, Wittig, and Related Enolate Reactions

  18. Selectivity and Reactivity in Enolate Reactions: Control of Stereoselectivity

  19. Radicals: Halogenation, Polymerization, and Reduction Reactions

  20. Reactions Controlled by Orbital Interactions: Ring Closures, Cycloadditions, and Rearrangements

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Tags: Ghis William Ogilvie, Nathan Ackroyd, Scott Browning, Organic, mechanistic

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