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1) Draw 3 different Lewis structures for a compound with the molecular formula C6H14O; then draw both the condensed formula and the line-angle structure for each.
2) Use resonance structures to show why acetate (CH3COO-) is more stable than ethoxide (CH3CH2O-); what does this say about the relative acidity of acetic acid and ethanol (their respective conjugate acids)?
Show all the steps in the mechanism for the following reaction, When benzene is mixed with deuterated sulfuric acid, deuterium is slowly incorporated onto the ring. Show the mechanism for this reaction and explain how this relates the sulfonation of ..
This assignment inhibits chemistry Laboratory Questions.
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Integrals for some of the resonances in the 1H NMR spectrum are higher than they should be due to the shear number of hydrogens in this compound
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