Organic Chemistry (6th Edition)
6th Edition
ISBN: 9781260119107
Author: Janice Gorzynski Smith
Publisher: McGraw Hill Education
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What is the likely mechanism of nucleophilic substitution for each alkyl halide?
What alkyl halide and nucleophile are needed to prepare each compound?
Draw the products formed when p-methylaniline (p-CH3C6H4NH2) istreated with following reagent.
Part (b), then CH3COCl, AlCl3
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- Draw the products formed when p-methylaniline (p-CH3C6H4NH2) istreated with following reagent. CH3COCl, AlCl3arrow_forwardThe ether, CH3OCH2CH3, can be prepared by two different nucleophilic substitution reactions, one using CH3O- as nucleophile and the other using CH3CH2O- as nucleophile. Draw both routes.arrow_forwardRank the following compounds in order of increasing reactivity in nucleophilic addition.arrow_forward
- Rank the following compounds in order of increasing reactivity toward nucleophilic attack.arrow_forwardRank the compounds in each group in order of increasing reactivity toward nucleophilic attack.arrow_forwardDraw the tautomer of this enol. Include all lone pairs. Ignore inorganic byproducts. :OH: :0: H3O+ Draw Tautomerarrow_forward
- Explain why benzaldehyde is less reactive than cyclohexanecarbaldehyde toward nucleophilic attack.arrow_forwardRank the compounds in each group in order of increasing reactivity in nucleophilic acyl substitution. CH3CH2CO2H, (CH3CH2CO)2O, CH3CH2CONHCH3arrow_forwardDraw two enol forms of the following diketone.arrow_forward
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