1. Draw the final product of the following reaction OH PBt3 2. A key precursor step...
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...
Draw the product of the reaction below: 0-CH2-CH2-CH3 H3C-CH2-CH2-CH ÓH H3C-CH2-CH2-OH = + H20
Draw the product to the reaction below. 13C-0-HC CH3 + H3C-CH2-OH CH3 about us careers privacy policy Draw the correct product for the reaction below. H3C—C—C— CH2-CH2-CH3 + H, → Draw the product to the reaction below. CH3 C + H₂C-OH CH₃
Draw the structure of the major product of the following acid-catalyzed dehydration. Question 4 CH3 H2804 H3C H3C CH3 heat OH Create OscerSketch Answer 4 Draw the major product of the following reaction. Question 5 CI-S-CH3 ~ I Нас pyridine Create OscerSketch Answer 5
Draw the product to the reaction below: -CH3-CH2 CH3 + i H3C—C—HC CH3 + CH3 H3C—CH2-OH CH3
Draw the product of the following reaction between a ketone and an alcohol. Include hydrogen atoms in your structural formula. он + H3C-¢-CH3 + HO-CH2-CH3 6-CH2-CH3 How would you classify the product of the reaction? It is an alcohol. + H20 It is a ketone. It is a hemiacetal. It is an acetal.
racemiC 3. In each of the following problems, draw a starting material that could be used as a suitable precursor in the conversion to the given product. a. b. H3C CN 1. CH3CO3H 1. TsCI, pyridine 2. H'/H20 он 2. NaCN, DMSO racemic d. CH3 H CH2 1. Br2, hv 1. HBr, CH3CO2H 2. KOCH3 2. KOtBu, DMSO
Please describe how each reaction will be accomplished. Alkyne and Nitrile Synthesis Retrosynthesis CH CH2 OH ОН Br HCECH + Synthesis CH CH2 0,0 NMO HCOCH Li NH NaNH Benzyl bromide OH OH Retrosynthesis One-on-o EN Br Synthesis Br KCN er blan NH2 H3C 1) LAH 2) H30* NH CH3 Alkyne and Nitrile Synthesis Retrosynthesis CH CH2 OH OH Br H2=CH + Synthesis CH CH2 0.0 NMO Li NH, NaNH, Benzyl bromide HC SCH OH OH The starting material is...
Multi-step synthesis ci R R NH, OEt А OH B 1. Br2 / uv light 2. SOCI2 / THE 3. Mg/Et20 4. Meu/hexane S. CH3CH2MgCl 6. Ph MgBe 7. NaBHA 8. LAHA 9. BH3 /OX 10. POCl/pyridine/ THF 11.03/THE 12. PCC / CH2 13.H/H20 14. ELOH/H 15. t-butaxide 16. OH/H20 17. NHS 18.CO2 19. acetic anhydride 20.HNMez/THE In each box, type out the list of reagents in proper order that will carry out the synthesis of the final product (This...
Please answer tbe following with explanations of why the reactions are occuring. Draw the salt produced in this reaction. Include all charges. O KOH © Draw the organic product on the reaction * Draw the final organic product of the reaction OH CH3 CH2 NH2 H2O + heat U draw the organic product of the reaction 3 유 H3C - CH-C-OH (H3C - CH - CH2 - CH2-OH CH₂ot