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3. Complete the following scheme. Two step reactions will contain two boxes. 5 points AKI 3....
Complete the following scheme. Two step reactions will contain two boxes. MgBr H AICI: 2. H 3. PCC, CH.CZ O H 2. H 3. H.CO OH 1. OH 2. Final product shows strong absorbance at 1700 cm-1 H-NMR singlet located downstream - 13.5 ppm H H Final product shows a strong absorbance at 1 700 cm-1 H-NMR signal located downstream-9.72 ppm АІСІ,
Please help me complete this. Two-step reactions will contain two boxes. 1. MgBr CI HI H AICI 2. H 3. PCC, CH.CH 1 . "H 2. H 3. H.CO OH 1. OH 2 Final product shows strong absortance at 1700 cm. H-NMR single located downstrom - 13.5 ppi H H Final product shows a strong absorbance at 1700 cm-1 H-NMR signal located downstream-9.72 ppm AICI
2. Give the products for the following aldol reactions. (5 points each) 1. Д. ОН: Н 2. н* 3. ОН: Н ОН ".. 5. ОН + CHO 6. ОН 3. Complete the following scheme. Two step reactions will contain two boxes. 5 points MgBr H CI 5 points AICI: 2. H 3. PCC, CH2Cl2 2 points 5 points 2 points 2. H 3. H Cr04 2 points 5 points OH 2 points 1. OH 5 points Final product shows strong...
(5) (9 points) Reactions involving aldehydes and ketones. In the text boxes below, indicate the most Teasonable product(s) for each reaction from the list of structures (A-H) in the box at the right. H.CO - YY (b) Product from (a) + TH
Complete the following questions/reactions by providing the missing portions shown by empty boxes. In some cases, not all boxes may be used or necessary. Show all major organic products unless otherwise specified. Make sure to clearly indicate stereochemistry where necessary CH, OH OH OH Br MgBr OH но CH, C AICI, KMnO4, H2O HC heat CHE 6363638 (CH,CH, Culi
1. Draw the products of each of the four steps in the designated boxes (5 points per box). step 1 step 2 PCC step 3 2) H20, H step 4 NaOCH, CH, OH Product 2. Draw a detailed mechanism for the transformations shown in: a) Step 2 (5 points): - b) Step 3 (5 points) c) Step 4 (5 points):
Complete the following reactions with the miss reagents(s) or major product(s). Br Hint: This Scheme involves Williamson Synthesis Xorph Ph HI (excess) OH
1) Complete the following reactions OH OH H2SO (b) (c) H2SO4 H,SO heat heat heat OH OH H.CO H.COM H.CO. OH f) 2) Show how to convert (a) 1-Propanol to 2-propanol in two steps (b) Cyclohexene to cyclohexanone in two steps (c) Propene to propanone (acetone) in two steps. 3) Write a stepwise mechanism for the sulfonation of benzene. Use HSO3 + as the electrophile.
Organic 2, aromatic reaction worksheet. Predicting the product or prodcuts of the reactions shown. CHEM 222 Aromatic Reaction Worksheet. Complete all problems 1.1 Predict the product or products of the reactions shown (if any) --CHy + HNO, H,SO -NO, CHE-CH-CH,-a AICI, Carmen FeBry -OH + Bry 1) HNO, H,SO 2) Fe, H3O+ 3) NaNO, HICT 4) CuCN -SO, H dil H,so AICI, H.CO (CH,),CHCH,CI Zn [Hg) ol... HCI, heat
Question 5. (16 marks) Complete the reactions to show the multi-step syntheses of each product. Reaction conditions go in boxes above arrows (1 reaction/box). Complete the template molecules provided in each box to show each step of the synthesis. Hint This question involves addition, elimination, substitution and alcohol chemistry а) Br (R)-2-bromo-3-methylbutanc но. CN (1-cyano-3-methylbutan-1-ol b) 2-methylbut-2-ene 2-methylbut-1-ene но. Page 10 of 11