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Solutions for Chapter 24: Carbohydrates

Organic Chemistry,  - Standalone Book | 2nd Edition | ISBN: 9781118452288 | Authors: David R. Klein

Full solutions for Organic Chemistry, - Standalone Book | 2nd Edition

ISBN: 9781118452288

Organic Chemistry,  - Standalone Book | 2nd Edition | ISBN: 9781118452288 | Authors: David R. Klein

Solutions for Chapter 24: Carbohydrates

Solutions for Chapter 24
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Textbook: Organic Chemistry, - Standalone Book
Edition: 2
Author: David R. Klein
ISBN: 9781118452288

Organic Chemistry, - Standalone Book was written by and is associated to the ISBN: 9781118452288. Chapter 24: Carbohydrates includes 87 full step-by-step solutions. This textbook survival guide was created for the textbook: Organic Chemistry, - Standalone Book, edition: 2. This expansive textbook survival guide covers the following chapters and their solutions. Since 87 problems in chapter 24: Carbohydrates have been answered, more than 67181 students have viewed full step-by-step solutions from this chapter.

Key Chemistry Terms and definitions covered in this textbook
  • accuracy

    A measure of how closely individual measurements agree with the correct value. (Section 1.5)

  • Alkoxy group

    An !OR group where R is an alkyl group

  • Amorphous domain

    A disordered, noncrystalline region in the solid state of a polymer.

  • amorphous solid.

    A solid that lacks a regular three-dimensional arrangement of atoms or molecules. (11.7)

  • cathode

    An electrode at which reduction occurs. (Section 20.3)

  • condensed structure

    A drawing style in which none of the bonds are drawn. Groups of atoms are clustered together when possible. For example, isopropanol has two CH3 groups, both of which are connected to the central carbon atom, shown like this: (CH3)2CHOH.

  • 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)

  • fuel cell

    A voltaic cell that utilizes the oxidation of a conventional fuel, such as H2 or CH4, in the cell reaction. (Section 20.7)

  • Glycol

    A compound with hydroxyl (!OH) groups on adjacent carbons.

  • Hydrophobic

    From the Greek, meaning water-fearing.

  • Lewis structures

    A drawing style inwhich the electrons take center stage.linear polymer (Sect. 27.6): A polymer thathas only a minimal amount of branching or nobranching at all.

  • mass number

    The sum of the number of protons and neutrons in the nucleus of a particular atom. (Section 2.3)

  • osmotic pressure

    The pressure that must be applied to a solution to stop osmosis from pure solvent into the solution. (Section 13.5)

  • oxidation–reduction (redox) reaction

    A chemical reaction in which the oxidation states of certain atoms change. (Section 4.4; Chapter 20: Introduction)

  • reactant

    A starting substance in a chemical reaction; it appears to the left of the arrow in a chemical equation. (Section 3.1)

  • secondary alkyl halide

    An organohalide in which the alpha (a) position is connected to exactly two alkyl groups.

  • sp3-hybridized orbitals

    Atomic orbitals that are achieved by mathematically averaging one s orbital with three p orbitals to form four hybridized atomic orbitals.

  • structural proteins

    Fibrous proteins that are used for their structural rigidity. Examples include a-keratins found in hair, nails, skin, feathers, and wool.

  • Tertiary structure of proteins

    The three-dimensional arrangement in space of all atoms in a single polypeptide chain.

  • Watson-Crick model

    A double-helix model for the secondary structure of a DNA molecule

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