×
Log in to StudySoup
Get Full Access to Chemistry - Textbook Survival Guide
Join StudySoup for FREE
Get Full Access to Chemistry - Textbook Survival Guide

Solutions for Chapter 2.4SE: Chemistry: The Central Science 13th Edition

Chemistry: The Central Science | 13th Edition | ISBN: 9780321910417 | Authors: Theodore E. Brown; H. Eugene LeMay; Bruce E. Bursten; Catherine Murphy; Patrick Woodward; Matthew E. Stoltzfus

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

ISBN: 9780321910417

Chemistry: The Central Science | 13th Edition | ISBN: 9780321910417 | Authors: Theodore E. Brown; H. Eugene LeMay; Bruce E. Bursten; Catherine Murphy; Patrick Woodward; Matthew E. Stoltzfus

Solutions for Chapter 2.4SE

Solutions for Chapter 2.4SE
4 5 0 386 Reviews
15
1

This textbook survival guide was created for the textbook: Chemistry: The Central Science, edition: 13. This expansive textbook survival guide covers the following chapters and their solutions. Chapter 2.4SE includes 2 full step-by-step solutions. Chemistry: The Central Science was written by and is associated to the ISBN: 9780321910417. Since 2 problems in chapter 2.4SE have been answered, more than 258034 students have viewed full step-by-step solutions from this chapter.

Key Chemistry Terms and definitions covered in this textbook
  • activity series.

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

  • bromonium ion

    A positively charged, bridged intermediate formed during the addition reaction that occurs when an alkene is treated with molecular bromine (Br2).

  • Center of symmetry

    A point so situated that identical components of an object are located on opposite sides and equidistant from that point along any axis passing through it.

  • coordination sphere

    The metal ion and its surrounding ligands. (Section 23.2)

  • Diastereotopic groups

    Atoms or groups on an atom that are bonded to an atom that is bonded to two nonidentical groups, one of which contains a chiral center. When one of the atoms or groups is replaced by another group, a new chiral center is created and a set of diastereomers results. The hydrogens of the CH2 group of 2-butanol, for example, are diastereotopic. Diastereotopic groups have different chemical shifts under all conditions

  • donor atom

    The atom of a ligand that bonds to the metal. (Section 23.2)

  • electrophilic aromatic substitution

    A substitution reaction in which an aromatic proton is replaced by an electrophile and the aromatic moiety is preserved.

  • Enol

    A compound containing a hydroxyl group bonded to a doubly bonded carbon atom.

  • Fischer projections

    A drawing style that is often used when dealing with compounds bearing multiple chirality centers, especially for carbohydrates. (See also Sect. 5.7.)

  • Haworth projection

    For substituted cycloalkanes, a drawing style used to clearly identify which groups are above the ring and which groups are below the ring. (See also Sect. 4.14.)

  • hydrocarbons

    Compounds composed of only carbon and hydrogen. (Section 2.9)

  • integration

    In 1H NMR spectroscopy, the area under a signal indicates the number of protons giving rise to the signal.

  • isoelectronic series

    A series of atoms, ions, or molecules having the same number of electrons. (Section 7.3)

  • Lactam

    A cyclic amide.

  • nematic liquid crystalline phase

    A liquid crystal in which the molecules are aligned in the same general direction, along their long axes, but in which the ends of the molecules are not aligned. (Section 11.7)

  • phase change

    The conversion of a substance from one state of matter to another. The phase changes we consider are melting and freezing 1solid ? liquid2, sublimation and deposition, and vaporization and condensation 1liquid ? gas2. (Section 11.4)

  • redox (oxidation–reduction) reaction

    A reaction in which certain atoms undergo changes in oxidation states. The substance increasing in oxidation state is oxidized; the substance decreasing in oxidation state is reduced. (Section 4.4; Chapter 20: Introduction)

  • sp2 Hybrid orbital

    A hybrid atomic orbital formed by the combination of one s atomic orbital and two 2p atomic orbitals.

  • stretching

    In IR spectroscopy, atype of vibration that generally produces a signal in the diagnostic region of an IR spectrum.

  • 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.

×
Log in to StudySoup
Get Full Access to Chemistry - Textbook Survival Guide
Join StudySoup for FREE
Get Full Access to Chemistry - Textbook Survival Guide
×
Reset your password