The nitro substituent was introduced in meta position of
Question- The nitro substituent was introduced in meta position of the methyl benzoate in nitration of methyl benzoate. Why does it prefer the meta position and not ortho and para?
Illustrate structures to prove your rezoning.
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problem- explain why shielding is more effective by electrons in a shell or lower principal quantum number than by
question- in the nitration of methyl benzoate yields of product were moderate at bestpart 1 which undesired products
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problem- set up the appropriate equations to solve for the speciation of the following system to a 1 l beaker of water
question- the nitro substituent was introduced in meta position of the methyl benzoate in nitration of methyl benzoate
problem- in the nitration of methyl benzoate why is it important to use cold methanol to wash the crude productstate
question- in the nitration of methyl benzoate what removes the hydrogen from the sp3 carbon in cationic reaction
problem- consider the following reaction in a closed reaction flask if 100 atm of gas a is allowed to react with 100
question- a 1000l sample has hcl gas at 25 c and 7320mmhg was absorbed completely in an aqueous solution that contained
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