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- Follow the curved arrows and draw the hydrocarbon product of the following reaction. Include all lone pairs and charges as appropriate. Ignore inorganic byproducts.What is the answer?Select the keyword or phrase that will best complete each sentence. Key terms: Toluene reacts faster than benzene in all substitution reactions. Thus, its electron- CH, group the benzene ring to acid electrophilic attack. activates A resonance effect is electron when resonance structures place a negative charge on carbons of the benzene ring. base k deactivates Inductive effects stem from the of the atoms in the substituent and the of the substituent groups. donating In a Friedel-Crafts alkylation, benzene is treated with an alkyl halide and a Lewis donation (AICI) to form an alkyl benzene. electronegativity nces When a neutral O or N atom is bonded directly to a benzene ring, the effect dominates and the net effect is electron inductive polarizability Nitrobenzene reacts more slowly than benzene in all substitution reactions. Thus, NO, group its electron- the benzene ring. poor A resonance effect is electron positive charge on carbons of the benzene ring. resonance when resonance…
- Complete the electron‑pushing mechanism for the given base‑promoted hydrolysis of an ester. Add atoms, bonds, nonbonding electron pairs (lone pairs), charges, and curved arrows where indicated.NoneComplete the following table to show what functional groups are present in each of the reagents and products in the reaction shown in ? (The first reagent has been filled in for you) Reagent / Product Functional group octanoic acid
- How will I determine if a neutral compound is an eletrophile or a nucleophilePart A Why do aldehydes undergo nucleophilic addition reactions while esters undergo nucleophilic acyl substitution reactions?Draw the appropriate reagents and solvent above and or below the arrow necessary to conduct the following reactions.
