Make up to $500 this semester by taking notes for StudySoup as an Elite Notetaker Apply Now
> > Organic Chemistry, 6

Organic Chemistry, 6th Edition - Solutions by Chapter

Organic Chemistry, | 6th Edition | ISBN: 9781429204941 | Authors: K. Peter C. Vollhardt Neil E. Schore

Full solutions for Organic Chemistry, | 6th Edition

ISBN: 9781429204941

Organic Chemistry, | 6th Edition | ISBN: 9781429204941 | Authors: K. Peter C. Vollhardt Neil E. Schore

Organic Chemistry, | 6th Edition - Solutions by Chapter

Solutions by Chapter
4 5 0 383 Reviews
Textbook: Organic Chemistry,
Edition: 6
Author: K. Peter C. Vollhardt Neil E. Schore
ISBN: 9781429204941

This expansive textbook survival guide covers the following chapters: 26. The full step-by-step solution to problem in Organic Chemistry, were answered by Patricia, our top Chemistry solution expert on 01/30/18, 05:11PM. Since problems from 26 chapters in Organic Chemistry, have been answered, more than 3169 students have viewed full step-by-step answer. This textbook survival guide was created for the textbook: Organic Chemistry,, edition: 6. Organic Chemistry, was written by Patricia and is associated to the ISBN: 9781429204941.

Key Chemistry Terms and definitions covered in this textbook
  • Activating group

    Any substituent on a benzene ring that causes the rate of electrophilic aromatic substitution to be greater than that for benzene.

  • alditol

    The product obtained when the aldehyde group of an aldose is reduced.

  • Alkylation reaction

    Any reaction in which a new carbon-carbon bond to an alkyl group is formed.

  • amphoteric oxides and hydroxides

    Oxides and hydroxides that are only slightly soluble in water but that dissolve in either acidic or basic solutions. (Section 17.5)

  • Anomeric carbon

    The hemiacetal or acetal carbon of the cyclic form of a carbohydrate

  • atomic number

    The number of protons in the nucleus of an atom of an element. (Section 2.3)

  • atomic weight

    The average mass of the atoms of an element in atomic mass units (amu); it is numerically equal to the mass in grams of one mole of the element. (Section 2.4)

  • Boat conformation

    A nonplanar conformation of a cyclohexane ring in which carbons 1 and 4 of the ring are bent toward each other

  • exo

    In Diels-Alder reactions that produce bicyclic structures, the positions that are anti to the larger bridge.

  • Geminal coupling

    Spin-spin coupling that occurs between nonequivalent H atoms bonded to the same C atom. The H atoms are generally nonequivalent owing to restricted bond rotation in the molecule

  • gray (Gy)

    The SI unit for radiation dose

  • Haber process

    The catalyst system and conditions of temperature and pressure developed by Fritz Haber and coworkers for the formation of NH3 from H2 and N2. (Section 15.2)

  • Infrared active

    Any molecular vibration that leads to a substantial change in dipole moment and is observed in an IR spectrum.

  • orbital

    An allowed energy state of an electron in the quantum mechanical model of the atom; the term orbital is also used to describe the spatial distribution of the electron. An orbital is defined by the values of three quantum numbers: n, l, and ml (Section 6.5)

  • oxyacid

    A compound in which one or more OH groups, and possibly additional oxygen atoms, are bonded to a central atom. (Section 16.10)

  • polarimeter

    A device that measures the rotation of plane-polarized light caused by optically active compounds.

  • primary cell

    A voltaic cell that cannot be recharged. (Section 20.7)

  • Principle of microscopic reversibility

    This principle states that the sequence of transition states and reactive intermediates in the mechanism of any reversible reaction must be the same, but in reverse order, for the reverse reaction as for the forward reaction

  • resonance structures

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

  • 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 Organic Chemistry,

Forgot password? Reset password here

Join StudySoup for FREE
Get Full Access to Organic Chemistry,
Join with Email
Already have an account? Login here
Forgot password? Reset your password here

I don't want to reset my password

Need help? Contact support

Need an Account? Is not associated with an account
Sign up
We're here to help

Having trouble accessing your account? Let us help you, contact support at +1(510) 944-1054 or support@studysoup.com

Got it, thanks!
Password Reset Request Sent An email has been sent to the email address associated to your account. Follow the link in the email to reset your password. If you're having trouble finding our email please check your spam folder
Got it, thanks!
Already have an Account? Is already in use
Log in
Incorrect Password The password used to log in with this account is incorrect
Try Again

Forgot password? Reset it here