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Chemistry: The Central Science 13th Edition - Solutions by Chapter

Chemistry: The Central Science | 13th Edition | ISBN: 9780321910417 | Authors: Theodore E. Brown

Full solutions for Chemistry: The Central Science | 13th Edition

ISBN: 9780321910417

Chemistry: The Central Science | 13th Edition | ISBN: 9780321910417 | Authors: Theodore E. Brown

Chemistry: The Central Science | 13th Edition - Solutions by Chapter

Solutions by Chapter
4 5 0 277 Reviews
Textbook: Chemistry: The Central Science
Edition: 13
Author: Theodore E. Brown
ISBN: 9780321910417

This expansive textbook survival guide covers the following chapters: 305. The full step-by-step solution to problem in Chemistry: The Central Science were answered by Sieva Kozinsky, our top Chemistry solution expert on 09/04/17, 09:30PM. Chemistry: The Central Science was written by Sieva Kozinsky and is associated to the ISBN: 9780321910417. This textbook survival guide was created for the textbook: Chemistry: The Central Science, edition: 13. Since problems from 305 chapters in Chemistry: The Central Science have been answered, more than 73776 students have viewed full step-by-step answer.

Key Chemistry Terms and definitions covered in this textbook
  • alkene

    A compound that possesses a carbon-carbon double bond.

  • Antiaromatic compound

    A monocyclic compound that is planar or nearly so, has one 2p orbital on each atom of the ring, and has 4n p electrons in the cyclic arrangement of overlapping 2p orbitals, where n is an integer. Antiaromatic compounds are especially unstable

  • benzyne

    A high-energy intermediate formed during the elimination-addition reaction that occurs between chlorobenzene and either NaOH (at high temperature) or NaNH2.

  • C-Terminal amino acid

    The amino acid at the end of a polypeptide chain having the free !COOH group.

  • Cis, trans isomers

    Stereoisomers that have the same connectivity but a different arrangement of their atoms in space as a result of the presence of either a ring or a carboncarbon double bond.

  • Constitutional isomers

    Compounds with the same molecular formula but a different connectivity of their atoms

  • coplanar

    Atoms that lie in the same plane.

  • Diaxial interactions

    Refers to the steric strain arising from interaction between an axial substituent and an axial hydrogen (or other group) on the same side of a chair conformation of a cyclohexane ring

  • ester

    An organic compound that has an OR group attached to a carbonyl; it is the product of a reaction between a carboxylic acid and an alcohol. (Section 24.4)

  • formal charge

    A charge associated with any atom that does not exhibit the appropriate number of valence electrons.

  • glucose

    A polyhydroxy aldehyde whose formula is CH2OH1CHOH24CHO; it is the most important of the monosaccharides. (Section 24.8)

  • heat of sublimation

    The enthalpy change, ?H, for vaporization of a solid. (Section 11.4)

  • hybrid orbital

    An orbital that results from the mixing of different kinds of atomic orbitals on the same atom. For example, an sp3 hybrid results from the mixing, or hybridizing, of one s orbital and three p orbitals. (Section 9.5)

  • Hückel criteria for aromaticity

    To be aromatic, a monocyclic compound must have one 2p orbital on each atom of the ring, be planar or nearly so, and have (4n 1 2) p electrons in the cyclic arrangement of 2p orbitals

  • Keq

    A term that describes the position of equilibrium for a reaction: Keq = 3H3O+ 4 3A- 4 3HA4 3H2O4

  • parts per million (ppm)

    The concentration of a solution in grams of solute per 106 (million) grams of solution; equals milligrams of solute per liter of solution for aqueous solutions. (Section 13.4)

  • Reactive intermediate

    A high-energy species formed between two successive reaction steps, that lies in an energy minimum between the two transition states

  • Tautomers

    Constitutional isomers in equilibrium with each other that differ in the location of a hydrogen atom and a double bond relative to a heteroatom, most commonly O, N, or S.

  • transport protein

    A protein used to transport molecules or ions from one location to another. Hemoglobin is a classic example of a transport protein, used to transport molecular oxygen from the lungs to all the tissues of the body.

  • triglyceride

    A triester formed from glycerol and three long-chain carboxylic acids.

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