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Ethyl m-nitrobenzoate

The simplest possible use that can be made of the Hammett equation is to calculate k or K for a specific reaction of a specific compound, where this information is not available in the literature, or indeed where the actual compound has not even been prepared yet. Thus it is known that the base-catalysed hydrolysis of ethyl m -nitrobenzoate is 63-5 times as fast as the hydrolysis of the corresponding unsubstituted ester under parallel conditions what then will be the comparable rate for base-catalysed hydrolysis of ethyl p-methoxybenzoate under the same conditions Looking at the table of [Pg.374]

The nitration method is also adaptable to the preparation of ethyl m-nitrobenzoate. The yield is, however, slightly lower, owing to the greater solubility of the ethyl ester. [Pg.72]

Ethyl o-nitrobenzoate Methyl o-nitrobenzoate Ethyl m-nitrobenzoate Methyl m-nitrobenzoate Ethyl p-nitrobenzoate Methyl p-nitrobenzoate... [Pg.1358]

See other pages where Ethyl m-nitrobenzoate is mentioned: [Pg.530]    [Pg.788]    [Pg.530]    [Pg.788]    [Pg.141]    [Pg.141]    [Pg.208]    [Pg.530]    [Pg.788]    [Pg.130]    [Pg.130]    [Pg.197]    [Pg.1386]    [Pg.1386]    [Pg.51]    [Pg.530]    [Pg.788]    [Pg.451]    [Pg.470]    [Pg.488]    [Pg.530]    [Pg.788]    [Pg.163]    [Pg.25]    [Pg.232]    [Pg.179]   
See also in sourсe #XX -- [ Pg.3 , Pg.72 ]



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Ethyl »,-nitrobenzoate

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