2. Study the third step (below) and answer the questions that follow. HO НО, ...OH X...
Which of the below reaction sequences will complete the transformation given? OH NH2 Ph1 PhV2 03 NaCN 1. LiAIH4 DMS HCN 2. H2O MCPBA NaN3 H2 Pt (111) 1. Oso PCC NH3, H2SO4 (cat.) 2. NaHSO3 NaBH3CN H2O (A) I, II only (B) I, III only (C) I only Question 14 An unknown compound exhibits the following is in the NMR spectrum 1.34ppm 3 405 om 2 7.17 om det 787 pom p om inget they the own compound (A)...
For the following questions, provide an answer based on what is
given.
Question 16: Can the molecule below be optically active? Why or why not? A. No because N has lone pair electrons. CN B. No because the molecule is symmetrical. C. Yes since the molecule cannot rotate and has 3D shape. D. Yes since the molecule has chiral centers. Question 17: Is the reaction correct or not? Why or why not? Me HO-Cr-OH Me H20, H2SO4 A. Reaction is...
use the notes provided to help answer the question
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The second step of the synthesis transformation of the chlorosulfonyl functional group into a sulfonamide) is an example of a a. Nucleophilic displacement (substitution) b Elimination C. Electrophilic aromatic substitution d. Acid hydrolysis Esterification e. THE SULFONIC ACID GROUP AND ITS DERIVATIVES Sulfonic acids are organic analogs of sulfuric acid, a very strong acid. They are highly corrosive, react vigorously with water, and can cause skin bums....