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> > Chemical Principles 8

Chemical Principles 8th Edition - Solutions by Chapter

Chemical Principles | 8th Edition | ISBN: 9781305581982 | Authors: Steven S. Zumdahl

Full solutions for Chemical Principles | 8th Edition

ISBN: 9781305581982

Chemical Principles | 8th Edition | ISBN: 9781305581982 | Authors: Steven S. Zumdahl

Chemical Principles | 8th Edition - Solutions by Chapter

This expansive textbook survival guide covers the following chapters: 20. Since problems from 20 chapters in Chemical Principles have been answered, more than 29901 students have viewed full step-by-step answer. The full step-by-step solution to problem in Chemical Principles were answered by , our top Chemistry solution expert on 12/23/17, 04:53PM. Chemical Principles was written by and is associated to the ISBN: 9781305581982. This textbook survival guide was created for the textbook: Chemical Principles, edition: 8.

Key Chemistry Terms and definitions covered in this textbook
  • alkoxide

    The conjugate base of an alcohol.

  • allylic bromination

    A radical reaction that achieves installation of a bromine atom at an allylic position.

  • anomeric carbon

    The C1 position of the cyclic hemiacetal of an aldose or the C2 position of the cyclic hemiacetal of a ketose.

  • Clemmensen reduction

    Reduction of the C"O group of an aldehyde or ketone to a CH2 group using Zn(Hg) and HCl

  • colligative properties.

    Properties of solutions that depend on the number of solute particles in solution and not on the nature of the solute particles. (12.6)

  • coupling (of protons)

    A phenomenon observed most commonly for nonequivalent protons connected to adjacent carbon atoms in which the multiplicity of each signal is affected by the other.

  • double helix

    The structure for DNA that involves the winding of two DNA polynucleotide chains together in a helical arrangement. The two strands of the double helix are complementary in that the organic bases on the two strands are paired for optimal hydrogen bond interaction. (Section 24.10)

  • epoxide

    A cyclic ether containing a three-membered ring system. Also called an oxirane (also see Sect. 14.7).

  • hydration

    A reaction in which a proton and a hydroxyl group (OH) are added across a p bond.

  • Keto-enol tautomerism

    A type of isomerism involving keto (from ketone) and enol tautomers

  • Low-density lipoprotein (LDL)

    Plasma particles, density 1.02–1.06 g/mL, consisting of approximately 26% proteins, 50% cholesterol, 21% phospholipids, and 4% triglycerides.

  • nitration

    An electrophilic aromatic substitution reaction that involves the installation of a nitro group (NO2) on an aromatic ring.

  • nonelectrolyte

    A substance that does not ionize in water and consequently gives a nonconducting solution. (Section 4.1)

  • phenolate

    The conjugate base of phenol or a substituted phenol.

  • plastic

    A material that can be formed into particular shapes by application of heat and pressure. (Section 12.8)

  • quaternary structure

    The structure of a protein resulting from the clustering of several individual protein chains into a final specific shape. (Section 24.7)

  • reducing sugar

    A carbohydrate that is oxidized upon treatment with Tollens’ reagent, Fehling’s reagent, or Benedict’s reagent.

  • solubility-product constant (solubility product)1Ksp2

    An equilibrium constant related to the equilibrium between a solid salt and its ions in solution. It provides a quantitative measure of the solubility of a slightly soluble salt. (Section 17.4)

  • Transition state

    The highest energy point on a reaction coordinate diagram. The chemical structure at this point is commonly called an activated complex.

  • Woodward-Fieser rules

    Rules for predicting the wavelength of maximum absorption for a compound with extended conjugation.

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