Solutions for Chapter 11: INTERMOLECULAR FORCES, LIQUIDS, AND SOLIDS

Chemistry: The Central Science | 11th Edition | ISBN: 9780136006176 | Authors: Theodore E. Brown, H. Eugene H LeMay, Bruce E. Bursten, Catherine Murphy, Patrick Woodward

Full solutions for Chemistry: The Central Science | 11th Edition

ISBN: 9780136006176

Chemistry: The Central Science | 11th Edition | ISBN: 9780136006176 | Authors: Theodore E. Brown, H. Eugene H LeMay, Bruce E. Bursten, Catherine Murphy, Patrick Woodward

Solutions for Chapter 11: INTERMOLECULAR FORCES, LIQUIDS, AND SOLIDS

Solutions for Chapter 11
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Textbook: Chemistry: The Central Science
Edition: 11
Author: Theodore E. Brown, H. Eugene H LeMay, Bruce E. Bursten, Catherine Murphy, Patrick Woodward
ISBN: 9780136006176

Since 97 problems in chapter 11: INTERMOLECULAR FORCES, LIQUIDS, AND SOLIDS have been answered, more than 7021 students have viewed full step-by-step solutions from this chapter. Chemistry: The Central Science was written by Patricia and is associated to the ISBN: 9780136006176. Chapter 11: INTERMOLECULAR FORCES, LIQUIDS, AND SOLIDS includes 97 full step-by-step solutions. This textbook survival guide was created for the textbook: Chemistry: The Central Science , edition: 11. This expansive textbook survival guide covers the following chapters and their solutions.

Key Chemistry Terms and definitions covered in this textbook
  • aldol addition reaction

    A reaction that occurs when an aldehyde or ketone is attacked by an enolate ion. The product of an aldol addition reaction is always a b-hydroxy aldehyde or ketone.

  • anomeric carbon

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

  • block copolymer

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

  • conjugated

    A compound in which two p bonds are separated from each other by exactly one s bond.

  • Dieckmann cyclization

    An intramolecular Claisen condensation.

  • dipole–dipole force

    A force that becomes significant when polar molecules come in close contact with one another. The force is attractive when the positive end of one polar molecule approaches the negative end of another. (Section 11.2)

  • Downfield

    A signal of an NMR spectrum that is shifted toward the left (larger chemical shift) on the chart paper.

  • Haloform

    A compound of the type CHX3 where X is a halogen.

  • Heterocycle

    A cyclic compound whose ring contains more than one kind of atom. Oxirane (ethylene oxide), for example, is a heterocycle whose ring contains two carbon atoms and one oxygen atom.

  • Hydrogen bonding

    The attractive interaction between a hydrogen atom bonded to an atom of high electronegativity (most commonly O or N) and a lone pair of electrons on another atom of high electronegativity (again, most commonly O or N).

  • Imine

    A compound containing a carbon-nitrogen double bond, R2C"NR’; also called a Schiff base

  • normal melting point

    The melting point at 1 atm pressure. (Section 11.6)

  • ozonolysis

    A reaction in which the CRC bond of an alkene is cleaved to form two CRO bonds.

  • primary structure

    The sequence of amino acids along a protein chain. (Section 24.7)

  • Prochiral hydrogens

    Refers to two hydrogens bonded to a carbon atom. When a different atom replaces one or the other, the carbon becomes a chiral center. The hydrogens of the CH2 group of ethanol, for example, are prochiral. Replacing one of them by deuterium gives (R)-1-deuteroethanol; replacing the other gives (S)-1-deuteroethanol

  • Protecting group

    Reversibly creating an unreactive group for the purpose of preventing a functional group from potentially reacting to give an unwanted product or products

  • reduction

    A reaction in which a compound undergoes a decrease in oxidation state.

  • Resonance

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

  • retro-aldol reaction

    The reverse of an aldol reaction. A b-hydroxyketone or aldehyde is converted into two ketones or aldehydes.

  • stretching

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

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