Can it please be drawn exactly!!!!! 
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Can it please be drawn exactly!!!!!
EXERCISE Resonance: Aromatic Substitution Clear _NO2 D-No OCHZ The nitration...
Nitration of phenols is a classic example of an electrophilic aromatic substitution reaction. a) Why does...
Nitration of phenols is a classic example of an electrophilic aromatic substitution reaction. a) Why does the nitration of phenol (hydroxybenzene) proceed only in the ortho- and para-positions on the ring? b) Draw the resonance structures that highlight the ortho- and para-directing nature of hydroxy substituents. Make sure to include the structures that showcase the movement of the charges in the ring.
EXERCISE Resonance: Allylic Cations Clear H3C -CH2CI HỌC -CH, Loss of chloride ion from 1-(chloromethyl)-4-methylcyclopentene (5)...
EXERCISE Resonance: Allylic Cations Clear H3C -CH2CI HỌC -CH, Loss of chloride ion from 1-(chloromethyl)-4-methylcyclopentene (5) produces an allylic carbocation that has two resonance structures Complete one of these resonance structures by dragging bonds, electrons and charges to the appropriate locations References) EXERCISE Resonance: Allylic Radicals Clear Η Η H3C Ally lic Radicals. Any radical in which the unpaired electron is on a carbon that is attached to a carbon-carbon double bond is an allylic radical For example, the structure...
2. Examine the following Electrophilic Aromatic Substitution reaction. 1) Provide the number of 13C NMR signals...
2. Examine the following Electrophilic Aromatic Substitution reaction. 1) Provide the number of 13C NMR signals expected in both the reactant and the product. 2) Provide the carbocation intermediate that allowed the transformation to happen at that position. 3) This molecule is (ortho, meta, para) substituted (circle one). 4) Using resonance arrows show how that carbocation can be distributed (delocalized) to multiple locations on the arene ring system. 5) Predict a different structure that can form from this delocalization. FeBrg,...
EXERCISE Resonance: Allylic Cations Clear H3C -CH2CI HỌC -CH, Loss of chloride ion from 1-(chloromethyl)-4-methylcyclopentene (5) produces an allylic carbocation that has two resonance structures Complete one of these resonance structures by dragging bonds, electrons and charges to the appropriate locations References) EXERCISE Resonance: Allylic Radicals Clear Η Η H3C Ally lic Radicals. Any radical in which the unpaired electron is on a carbon that is attached to a carbon-carbon double bond is an allylic radical For example, the structure...
2. Examine the following Electrophilic Aromatic Substitution reaction. 1) Provide the number of 13C NMR signals expected in both the reactant and the product. 2) Provide the carbocation intermediate that allowed the transformation to happen at that position. 3) This molecule is (ortho, meta, para) substituted (circle one). 4) Using resonance arrows show how that carbocation can be distributed (delocalized) to multiple locations on the arene ring system. 5) Predict a different structure that can form from this delocalization. FeBrg,...
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