RON C11H21NO, 2 R3NH Br NH2 Br A Treatment of 3-methylpentan-3-amine with methyl 2,4- dibromobutanoate in...
NH2 R3N Br C14H19NO2 + 2 R3NH Br Br A Treatment of 2-phenylpropan-2-amine with methyl 2,4-dibromobutanoate in the presence of a nonnucleophilic base, R3N, involves two successive Sn2 reactions and gives compound A. Propose a structural formula for compound A. You do not have to consider stereochemistry.
9.13 Draw a structural formula for the product of each S 2 reaction. Where configuration of the starting material is given, show the configuration of the product. (a) CH,CH,CH,Cl + CH,CH,O-Nat - (b) (CH3)3N + CHI acetone (c) CHBr + Na*CN- acetone CI + CH2S+Na+ - (d) HC ethanol (e) CHỊCH,CH,Cl + CHỤC=C Li* ( -chĄC + NH; echanol diethyl ether (g) 0 NH + CH3(CHỊ) CHỊC14 (h) CH CH.CH,Br + NaCN to acetone 9.16 Treatment of 1-aminoadamantane, CH, N,...
1. Name the following or Draw the Structure (2 x 3 pts each) a. N-methyl-3-phenylpentan-2-amine OH b. OH NH2O 2. Draw the starting materials for the following hydrolysis reactions. (3 pts each) 1. NaOH, H2O a. 3-or 2. HCI, H2O OH OH Ph 1. NaOH, H2O b. HO Н. CH3 OH HPh 2. HCI, H2O 3. Of the following, which form would actually exist at: (5 points) a) pH = 2 (acidic) b) pH = 7 (neutral) c) pH =...