Identify the product that forms at each step of the reaction sequence shown below. 5. Identify...
46) What is the major product formed in the 4-step reaction sequence? Io non o od NH C AICI NO2 2) H0 3) HNO3, H2SO4 4) H2NNH, KOH 47) What is the final product formed in the following sequence of reactions? NHCOCH3OH 1) H,SO./H201) NaNO,, HCI ? heat Conc. H,SO 2 ) H3PO, SOGH 2) dilute NaOH NH21 oor hoe oud SO,H 48) Which of the following reactions would occur as written? Select all that apply. O CHOCI Snc 1)...
19. Determine the major product from the following reaction sequence. 5 points i. HBF, H, COOCH, a 소 b HoL C. ii. KO'Bu, 'BuOH, A OH OH (CH3),C=CHCH, ? iii. BH, THE d e. НО. iv. H,O, NaOH OH a b с d e
b. What is the major product of the reaction sequence shown below? Show the intermediates in each step. What is the use of AlCl, in step 1 and step 2 structures of important 1. C. Aici 0 2. CI AICl, 3. Bry, FeBr
5. Predict the major product of the reaction shown below 0 H2NCH3, cat. H* CH3 (c) HNH H3C .сн он 0 CH3 .сн CH3 6. Predict the major product of the reaction shown below. H2NCH3, cat. H+ CH3 0 он CH3 CH3 CH3
Question 19 Identify the correct reactant necessary for the reaction shown below. Question 20 Which of the reactions shown below would be regioselective? (choose all correct answers) H-CI Bry, H,O Bra 1. BH3, H2O, THE 2. H2O2, OH, H2O
1. Identify the predominant mono-nitrated product expected to form in the following reaction. HNO3 - H2SO4 ? NO o CH3 O N o NO2 CH₂ CHE (B) (D) 8. Identify the product obtained on completion of the following reaction sequence. Assume that a racemic mixture is generated if the product contains asymmetric centers. Bry, H20 NaOH : NaCN, H2O (1 equivalent) он
What is the major product of the reaction sequence shown below? сненснен, ва , снсноке", CH3 CHCHCHCH, Bry CH3CH2O Na" light О2-methyl-1-butene 3-methyl-1-butene 2-methylbutane 2-methyl-2-butene
Identify the product X, formed by the reaction sequence shown. these steps were used in the Synthesis of resiniferaroxin, the complex chapter-opening molecule. 1744 Identity the product X, formed by the reaction sequence shown. These steps were used in the synthesis of resiniferatoxin, the complex chapter-opening molecule 19 POCO b ) OSR (CH), OSIR, 211 MgB 131 H 0 17.45 Draw all stereoisomers formed in each reaction
Draw all of the products formed in each reaction. Include all hydrogen atoms. Reaction A Select Draw Rings More Erase CH3 CH3 heat -CH OH + H- N Hąc CH₃ Reaction B Select Draw Rings More Erase CH HCI HH HVO Reaction C Select Draw Rings More Erase NaOH & H3C Hoo H O_H CHE Reaction D Select Draw Rings More Erase o=0 H CH + LiOH CHz - HO CH3 @ 212,
1 & 2) Draw the product to the reaction below. 3) Select the chiral atoms in the aspartame molecule. Draw the product to the reaction below: + OH CH3 H3C—_—HĆ-CH3 + H3C—CH2-OH 6-CH2-CH3 + H20 Draw the product to the reaction below: H3C-CH2-0 H3C—CH2—C—OH + CH3 H3C—CH2-OH + H20 Aspartame is a popular sugar substitute. It is 150 times sweeter than sucrose so very little is needed to sweeten foods. Identify the chirality center(s), sometimes called chiral carbon atoms, in...