synthesize the following 1 - RR t N NH2

Question

Question

synthesize the following

Answer 1

Answer #1

B is the base in the mechanism.

This reaction is an example of imine hydrolysis formed im Schiff Base reaction. The mechanism is shown below. H-B H xH + Nota

Answer 2

Similar Homework Help Questions

Which steps will be necessary to synthesize the peptide below? OH NH2 phenylalanine HO NH2 ОН...

Which steps will be necessary to synthesize the peptide below? OH NH2 phenylalanine HO NH2 ОН NH2 isoleucine 1. The N-terminus of isoleucine will require a deactivating protecting group. II. The N-terminus of phenylalanine will require a deactivating protecting group. III. The C-terminus of of isoleucine will require activation. IV. The C-terminus of phenylalanine will require activation. II and III II and IV I and III I and IV
199.9 NH2 HNO3 H,SO Synthesize each of the following beginning with benzene. google good

199.9 NH2 HNO3 H,SO Synthesize each of the following beginning with benzene. google good
Synthesize the following compounds from benzene. СООН b Br NO2 NO2 NH2 Br ОН СООН b...

Synthesize the following compounds from benzene. СООН b Br NO2 NO2 NH2 Br ОН СООН b Br NO2 NO2 NH2 Br ОН

3. Synthesize the following by showing all the appropriate reagents and intermediates. (6 pts b. CI...

3. Synthesize the following by showing all the appropriate reagents and intermediates. (6 pts b. CI -NH2 N OCH CI-
What reagent will perform the following transformation? NH2 CN N -NH2 H2N-NH2 + 20 с NH...

What reagent will perform the following transformation? NH2 CN N -NH2 H2N-NH2 + 20 с NH + NH3 о INH + NH3 оооооо
16) Which of the following is formed when 3-methylcyclopentanone reacts with hydroxylamine? A2N-NH-C6H5 N-NH2 N-OH IT...

16) Which of the following is formed when 3-methylcyclopentanone reacts with hydroxylamine? A2N-NH-C6H5 N-NH2 N-OH IT III 02 Daylen *NH H I Ź IV < 7) Which Wittig reagent would be used to synthesize CHẶCH=P(CH3), CH=P(CH3)3 P(CH3)3 CHșCH2CH=P(CH3)3 I IV a) I b) II c) III d) IV e) Either I or II could be used.

Show how you would synthesize the following a n d beginning with 1-butene, Bromma and any...

Show how you would synthesize the following a n d beginning with 1-butene, Bromma and any necessary additional reagents. More than one step is needed. Br Bromobenzene, 1-Butene < Show how you woull Synthesize 4.- Nonanone, begining with 1-Butanol and any other non-organic reagents. (1-Butanol is the only Organic compouno available). only organ n
The structure below represents a NH2 N N N N НО. OH A) nucleic acid B)...

The structure below represents a NH2 N N N N НО. OH A) nucleic acid B) nucleoside. C) glycoside. D) nucleotide. E) riboside. The structural arrangement of DNA is A) -ribose---phosphate-ribose---phosphate — 1 base base B) -ribose -phosphate-ribose-phosphate 1 base base C) -deoxyribose-base-deoxyribose -base- 1 phosphate phosphate D) -deoxyribose---phosphate — deoxyribo se —-phosphate- base base E) — deoxyribose – phosphate-deoxyribose – phosphate — 1 base base The heterocyclic compounds adenine (A) and thymine (T) form base pairs in DNA via...
Question 5 (1 point) Which of the following compounds is an amine? NH N- NH2 b...

Question 5 (1 point) Which of the following compounds is an amine? NH N- NH2 b a a b all of the above only b and c

3. Synthesize the following by showing all the appropriate reagents and intermediates. (6 pts.) b. a....

3. Synthesize the following by showing all the appropriate reagents and intermediates. (6 pts.) b. a. M -OCH3 CI -NH2