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Solutions for Chapter Lesson 78: Mass-Mole Conversions

Full solutions for Living by Chemistry | 2nd Edition

ISBN: 9781464142314

Solutions for Chapter Lesson 78: Mass-Mole Conversions

This textbook survival guide was created for the textbook: Living by Chemistry, edition: 2. Since 8 problems in chapter Lesson 78: Mass-Mole Conversions have been answered, more than 23228 students have viewed full step-by-step solutions from this chapter. Living by Chemistry was written by and is associated to the ISBN: 9781464142314. This expansive textbook survival guide covers the following chapters and their solutions. Chapter Lesson 78: Mass-Mole Conversions includes 8 full step-by-step solutions.

Key Chemistry Terms and definitions covered in this textbook
  • base.

    A substance that yields hydroxide ions (OH2) when dissolved in water. (2.7)

  • buffered solution (buffer)

    A solution that undergoes a limited change in pH upon addition of a small amount of acid or base. (Section 17.2)

  • carbohydrates

    Polyhydroxy aldehydes or ketones with molecular formula CxH2xOx.

  • chain reaction

    A series of reactions in which one reaction initiates the next. (Section 21.7)

  • chemistry

    The scientific discipline that studies the composition, properties, and transformations of matter. (Chapter 1: Introduction)

  • Clemmensen reduction

    A reaction in which a carbonyl group is completely reduced and replaced with two hydrogen atoms.

  • Clemmensen reduction

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

  • Dextrorotatory

    Refers to a substance that rotates the plane of polarized light to the right

  • frequency

    For electromagnetic radiation, the number of wavelengths that pass a particular point in space per unit time.

  • hydronium ion 1H3O+2

    The predominant form of the proton in aqueous solution. (Section 16.2)

  • indicator

    A substance added to a solution that changes color when the added solute has reacted with all the solute present in solution. The most common type of indicator is an acid–base indicator whose color changes as a function of pH. (Section 4.6)

  • Oxymercuration-reduction

    A method for converting an alkene to an alcohol. The alkene is treated with mercury(II) acetate followed by reduction with sodium borohydride.

  • pi 1P2 bond

    A covalent bond in which electron density is concentrated above and below the internuclear axis. (Section 9.6)

  • primary structure

    For proteins, the sequence of amino acid residues.

  • resonance structures

    A series of structures that are melded together (conceptually) to circumvent the inadequacies of bond-line drawings.

  • retrosynthetic analysis

    A systematic set of principles that enable the design of a synthetic route by working backward from the desired product.

  • solvolysis

    A substitution reaction in which the solvent functions as the nucleophile.

  • specific rotation

    For a chiral compound that is subjected to plane-polarized light, the observed rotation when a standard concentration (1 g/mL) and a standard path length (1 dm) are used.

  • thermodynamics

    The study of how energy is distributed under the influence of entropy. For chemists, the thermodynamics of a reaction specifically refers to the study of the relative energy levels of reactants and products.

  • waxes

    High-molecular-weight esters that are constructed from carboxylic acids and alcohols.

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