Solutions for Chapter 3.16: Fused Cyclohexane Rings

Organic Chemistry | 8th Edition | ISBN: 9780134042282 | Authors: Paula Yurkanis Bruice

Full solutions for Organic Chemistry | 8th Edition

ISBN: 9780134042282

Organic Chemistry | 8th Edition | ISBN: 9780134042282 | Authors: Paula Yurkanis Bruice

Solutions for Chapter 3.16: Fused Cyclohexane Rings

Solutions for Chapter 3.16
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Textbook: Organic Chemistry
Edition: 8
Author: Paula Yurkanis Bruice
ISBN: 9780134042282

This textbook survival guide was created for the textbook: Organic Chemistry, edition: 8. This expansive textbook survival guide covers the following chapters and their solutions. Chapter 3.16: Fused Cyclohexane Rings includes 35 full step-by-step solutions. Since 35 problems in chapter 3.16: Fused Cyclohexane Rings have been answered, more than 15368 students have viewed full step-by-step solutions from this chapter. Organic Chemistry was written by and is associated to the ISBN: 9780134042282.

Key Chemistry Terms and definitions covered in this textbook
  • Absorbance (A)

    A quantitative measure of the extent to which a compound absorbs radiation of a particular wavelength. A 5 log (I0/I ) where I0 is the incident radiation and I is the transmitted radiation

  • activity series.

    A summary of the results of many possible displacement reactions. (4.4)

  • acyl group

    The term describing a carbonyl group (CRO bond) connected to an alkyl group or aryl group.

  • Aldonic acid

    The product formed when the !CHO group of an aldose is oxidized to a !COOH group

  • aldose

    A carbohydrate that contains an aldehyde group.

  • azo dyes

    A class of colored compounds that are formed via azo coupling.

  • band structure

    The electronic structure of a solid, defining the allowed ranges of energy for electrons in a solid. (Section 12.7)

  • block copolymer

    A copolymer in which the different homopolymer subunits are connected together in one chain.

  • chemical equilibrium.

    A state in which the rates of the forward and reverse reactions are equal. (14.1)

  • constitutional isomers

    Compounds that have the same molecular formula but differ in the way the atoms are connected.

  • epimer

    Diastereomers that differ from each other in the configuration of only one chirality center.

  • lambda max (lmax)

    In UVVis spectroscopy, the wavelength of maximum absorption.

  • migratory aptitude

    In a BaeyerVilliger oxidation, the migration rates of different groups, which determine the regiochemical outcome of the reaction.

  • Nucleophilic aromatic substitution

    A reaction in which a nucleophile, most commonly a halogen, on an aromatic ring is replaced by another nucleophile.

  • polarimeter

    A device that measures the rotation of plane-polarized light caused by optically active compounds.

  • positron emission

    A nuclear decay process where a positron, a particle with the same mass as an electron but with a positive charge, symbol 0+1e, or b+ is emitted from the nucleus. (Section 21.1)

  • Resonance

    A theory that many molecules and ions are best described as a hybrid of several Lewis structures

  • Secondary structure of nucleic acids

    The ordered arrangement of nucleic acid strands

  • strong deactivators

    Groups that strongy deactivate an aromatic ring toward electrophilic aromatic substitution, thereby significantly decreasing the rate of the reaction.

  • tertiary structure

    The threedimensional shape of a protein.

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