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Chemistry
10th Edition
ISBN: 9781305957404
Author: Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Publisher: Cengage Learning
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
Transcribed Image Text:Choose the most appropriate reagent(s) for the conversion of the ketone to the primary amine
intermediate.
OH
NH2
Na Cr207
HSO4
HO
reagent (s)
N(CH3
H2, Pd
B)
NABH4,
CH3CH,OH
NANH2, NH3
1. LIAIH,
2. H, H20
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- What alkyl halide would be the starting reactant for this reaction? 1. Mg0 2. O ??? B с None of these A 3. H+ D (A) Br Br. H (B) Br (C) OH (D) Brarrow_forwardBased on concepts learned in the synthesis of lidocaine, what is the preferred product of the reaction below? NH2 CH;COOH , O A. 1 O B. there is no reaction OC.3 O D.2 QUESTION 13 The amide shown below is an intermediate product in the synthesis of lidocaine. It contains a nitrogen benzene ring, and a chlorine attached to a primary carbon, yet it doesn't react with itself in a nucleophil Why is this? Click Save and Submit to save and submit. Click Save All Ansuwers to save all answers. search F10 C F5 F9 + F3 F6 F4 F2 %23 % 3 Y CO O LOarrow_forwardB. Supply the missing product or reagent for the following reactions OH ОН OH PCC POCI3,, pyridine HBr, heat OH OH Br Mg H₂SO4, heat 1) NaH 2) Ph Brarrow_forward
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