- Chapter 1: S t r u c t u r e a n d B o n d i n g i n O r g a n i c M o l e c u l e s
- Chapter 10: U s i n g N M R S p e c t r o s c o p y t o D e d u c e S t r u c t u r e
- Chapter 11: S o l v i n g P r o b l e m s i n O r g a n i c C h e m i s t r y
- Chapter 12: R e a c t i o n s o f A l k e n e s
- Chapter 13: A l k y n e s
- Chapter 14: D e l o c a l i z e d P i S y s t e m s
- Chapter 15: B e n z e n e a n d A r o m a t i c i t y
- Chapter 16: E l e c t r o p h i l i c A t t a c k o n D e r i v a t i v e s o f B e n z e n e
- Chapter 17: A l d e h y d e s a n d K e t o n e s
- Chapter 18: E n o l s , E n o l a t e s , a n d t h e A l d o l C o n d e n s a t i o n
- Chapter 19: C a r b o x y l i c A c i d s
- Chapter 2: S t r u c t u r e a n d R e a c t i v i t y
- Chapter 20: C a r b o x y l i c A c i d D e r i v a t i v e s
- Chapter 21: A m i n e s a n d T h e i r D e r i v a t i v e s
- Chapter 22: C h e m i s t r y o f B e n z e n e S u b s t i t u e n t s
- Chapter 23: E s t e r E n o l a t e s a n d t h e C l a i s e n C o n d e n s a t i o n
- Chapter 24: E s t e r E n o l a t e s a n d t h e C l a i s e n C o n d e n s a t i o n
- Chapter 25: E s t e r E n o l a t e s a n d t h e C l a i s e n C o n d e n s a t i o n
- Chapter 26: A m i n o A c i d s , P e p t i d e s , P r o t e i n s , a n d N u c l e i c A c i d s
- Chapter 3: R e a c t i o n s o f A l k a n e s
- Chapter 4: C y c l o a l k a n e s
- Chapter 5: S t e r e o i s o m e r s
- Chapter 6: P r o p e r t i e s a n d R e a c t i o n s o f H a l o a l k a n e s
- Chapter 7: F u r t h e r R e a c t i o n s o f H a l o a l k a n e s
- Chapter 8: H y d r o x y F u n c t i o n a l G r o u p : A l c o h o l s
- Chapter 9: F u r t h e r R e a c t i o n s o f A l c o h o l s a n d t h e C h e m i s t r y o f E t h e r s
Organic Chemistry, 6th Edition - Solutions by Chapter
Full solutions for Organic Chemistry, | 6th Edition
ISBN: 9781429204941
Solutions by Chapter
This expansive textbook survival guide covers the following chapters: 26. The full step-by-step solution to problem in Organic Chemistry, were answered by , our top Chemistry solution expert on 01/30/18, 05:11PM. Since problems from 26 chapters in Organic Chemistry, have been answered, more than 7563 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 and is associated to the ISBN: 9781429204941.
Key Chemistry Terms and definitions covered in this textbook
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acidic cleavage
A reaction in which bonds are broken in the presence of an acid. For example, in the presence of a strong acid, an ether is converted into two alkyl halides.
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closed system.
A system that enables the exchange of energy (usually in the form of heat) but not mass with its surroundings. (6.2)
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complementary colors
Colors that, when mixed in proper proportions, appear white or colorless. (Section 23.5)
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condensation polymer
A polymer,that is formed via a condensation reaction.
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critical pressure
The pressure at which a gas at its critical temperature is converted to a liquid state. (Section 11.4)
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decomposition reaction.
The breakdown of a compound into two or more components. (4.4)
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electrolysis reaction
A reaction in which a nonspontaneous redox reaction is brought about by the passage of current under a sufficient external electrical potential. The devices in which electrolysis reactions occur are called electrolytic cells. (Section 20.9)
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electron
A negatively charged subatomic particle found outside the atomic nucleus; it is a part of all atoms. An electron has a mass 1>1836 times that of a proton. (Section 2.3)
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energy-level diagram
A diagram that shows the energies of molecular orbitals relative to the atomic orbitals from which they are derived. Also called a molecular-orbital diagram. (Section 9.7)
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enthalpy of reaction
The enthalpy change associated with a chemical reaction. (Section 5.4)
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Heat of combustion (DH0 )
Standard heat of combustion is the heat released when one mole of a substance in its standard state (gas, liquid, solid) is oxidized completely to carbon dioxide and water.
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Homolytic bond cleavage
Cleavage of a bond so that each fragment retains one electron; formation of radicals.
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hydrogen bonding
A special type of dipole-dipole interaction that occurs between an electronegative atom and a hydrogen atom that is connected to another electronegative atom.
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nonbonding pair
In a Lewis structure a pair of electrons assigned completely to one atom; also called a lone pair. (Section 9.2)
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Nuclear magnetic resonance (NMR) spectroscopy
A spectroscopic technique that gives information about the number and types of atoms in a molecule, for example, hydrogens (1 H!NMR) and carbons (13C!NMR)
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Peptide bond
The special name given to the amide bond formed between the a-amino group of one amino acid and the a-carboxyl group of another amino acid
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proton
A positively charged subatomic particle found in the nucleus of an atom. (Section 2.3)
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Restriction endonuclease
An enzyme that catalyzes the hydrolysis of a particular phosphodiester bond within a DNA strand.
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Triol
A compound containing three hydroxyl groups.
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zwitterion
A net neutral compound that exhibits charge separation. Amino acids exist as zwitterions at physiological pH.