a) In each of the five molecules listed below, circle the most acidic hydrogen. Be aware that you might have to explicitly draw out the hydrogen, as not all hydrogens are shown in skeletal notation. HO. OH B A b) In the box, write the letters for the molecule(s) that would form an enolate if treated with 1 eq of LDA at -78 °C in THF. C D NH₂ E
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- Chemistry Please help explain this textbook question: Although N, N -dimethylaniline is extremely reactive toward electrophilic aromatic substitution and is readily substituted by weak electrophiles, such as diazonium and nitronium ions, this reactivity is greatly diminished by the introduction of an alkyl substituent in an ortho position.Draw the major product of this reaction. Ingore any organic byproductsIn benzoic acid, when it has a deactivating group in position "para" (relative to carboxylate position) , it attracts electrons towards it, weakening the acid and an activator pushes the electrons making the acid stronger.What happens to this benzoic acid if it has a substituent at the "meta" or "ortho" position as an activator or a deactivator? I need an explanation of what happens in each case please
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