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19 Nov 2019
Hi, Iâm really having trouble understanding questions 2. (a,b,c,d,e,f) and 3.
2. Draw the major product(s) (showing appropriate stereochemistry when necessary) for the following reactions. Indicate the mechanism(s) in operation (SNI, SN2, El, or E2). Cl2ã 2. d. a. acetone CH2CH3 NaOCH2CH3 e. 2 NHs b. Br 2. Nal Br NaOCHa DMSO C. HOCH3 CH3 3. When 1-chloro-2-butene reacts in 50% aqueous acetone at 500, the product is a mixture of two alcohols CH,CH(OH)CH-CH2 CH,CH-CHCH,OH (56%) CH,CH-CHCH,CI> OR (44%) Write out a detailed MECHANISM that accounts for these experimental facts. (HINT: The intermediate is "resonance stabilized".)
Hi, Iâm really having trouble understanding questions 2. (a,b,c,d,e,f) and 3.
2. Draw the major product(s) (showing appropriate stereochemistry when necessary) for the following reactions. Indicate the mechanism(s) in operation (SNI, SN2, El, or E2). Cl2ã 2. d. a. acetone CH2CH3 NaOCH2CH3 e. 2 NHs b. Br 2. Nal Br NaOCHa DMSO C. HOCH3 CH3 3. When 1-chloro-2-butene reacts in 50% aqueous acetone at 500, the product is a mixture of two alcohols CH,CH(OH)CH-CH2 CH,CH-CHCH,OH (56%) CH,CH-CHCH,CI> OR (44%) Write out a detailed MECHANISM that accounts for these experimental facts. (HINT: The intermediate is "resonance stabilized".)
Jamar FerryLv2
25 May 2019