![Chemical Properties of Monocyclic Aromatic Hydrocarbons(5)](http://s1.studyres.com/store/data/008286659_1-430e115898ed9f5bb26e49e8ffd79e11-300x300.png)
Notes
... Definition/Functional group: contain at least one benzene ring, often with other groups added (“substituted” for hydrogen). Benzene exists as a resonance structure. It is also a carcinogen. Prefix: Benz Examples Benzene Benzaldehyde ...
... Definition/Functional group: contain at least one benzene ring, often with other groups added (“substituted” for hydrogen). Benzene exists as a resonance structure. It is also a carcinogen. Prefix: Benz Examples Benzene Benzaldehyde ...
Organic Chemistry: Introduction
... • August Kekule proposed a structure with a ring of C with alternating single and double bonds. • Unsymmetrical with different lengths of bonds. ...
... • August Kekule proposed a structure with a ring of C with alternating single and double bonds. • Unsymmetrical with different lengths of bonds. ...
Aromatic Compounds
... When electrons fill the various molecular orbitals, one pair of electrons fills the lowest-lying orbital and two pairs of electrons fill each of the n successive energy levels – a total of 4n + 2. Any other number would leave a bonding energy level partially unfilled Energy levels of the six benzene ...
... When electrons fill the various molecular orbitals, one pair of electrons fills the lowest-lying orbital and two pairs of electrons fill each of the n successive energy levels – a total of 4n + 2. Any other number would leave a bonding energy level partially unfilled Energy levels of the six benzene ...
Functional Groups
... then number chain to minimize position of second branch (and then third and so on). if still in need of a tie breaker, minimize # of substituent group that comes first alphabetically ...
... then number chain to minimize position of second branch (and then third and so on). if still in need of a tie breaker, minimize # of substituent group that comes first alphabetically ...
Arenes HW
... Explain why electrophiles, such as bromine, react much more readily with phenol than with benzene. ...
... Explain why electrophiles, such as bromine, react much more readily with phenol than with benzene. ...
Aromatic Compounds
... Comparison of electrophilic and nucleophilic aromatic substitution reactions • Electrophilic substitutions are favored by electrondonating substituents which stabilize the carbocation intermediate • Nucleophilic substitutions are favored by electronwithdrawing substituents which stabilize a carbanio ...
... Comparison of electrophilic and nucleophilic aromatic substitution reactions • Electrophilic substitutions are favored by electrondonating substituents which stabilize the carbocation intermediate • Nucleophilic substitutions are favored by electronwithdrawing substituents which stabilize a carbanio ...