ICA 11-21-2019 (CA Derivatives) Complete the following problems on your own paper. Rewrite the problem 1....
Complete the following problems on your own paper. Rewrite the problem. 1. Draw the answer to the following reactions. ao NOGO NaCrO Br 1. NaCN 2. H,O* 1. LiAlH 2. H30* 1. Mg 2. CO2 3. HO* 4. CH CH2CH2CH,OH, H2SO4(catalytic amount) 1. Na2Cr2O7. H SOHO 2. SOCI 3. (CHUCH CH2)2Culi OI 1. SOCI 2. CH CH OH Ο ΟΗ
Complete the following problems on your own paper. Rewrite the problem. Draw the answer to the following reactions. 1. NaCr O 1. CO2 2. Н,о. Mg Br 1. NaCN 2. H20 Br 1. LIAIH 2. H0 HO 1. Mg 2. CO2 3. Hy0 4. CH,CH2CH CH2OH, H2SOcatalytic amount) Br 1. Na2Cr O7, H2SO H20 2. SOCh 3. (CH2CH2CH22CuLi 1. SOC 2, CH,CH2OH он
ICA 11-19-2019 Carboxylic Acids Please complete the following assignment on your own paper 1. Name the following using IUPAC Naming. Br 1 ОН OH Br OH НО Name and Rank the following compounds as Most Acidic, Middle and Least Acidic OOH OH al O OH
Complete the follow problems on your own paper. Rewrite the problem and the answer. 1. Draw the product(s) of the following reactions H.CrO4 1. CH,COCVAICI: 2. Zn (Hg)/HCI 3. NBS (light) T 1. KMnO4/H,SO4 NaNH2 NH30 2. Show how you would synthesize the following compounds from toluene. оон Br
Complete the follow problems on your own paper. Rewrite the problem and the answer. 1. Draw the product(s) of the following reactions HyCro 1. CH,COCTAICI 2. Zn (Hg)/HCI 3. NBS (light) 1. KMnO4/H2SO4 NaNH2 NH3(0) 2. Show how you would synthesize the following compounds from toluene. Br
1. Draw the answer to the following reactions. Dr NaCr2O7 NaClO Br 1. NaCN 2. H2O* www . Dan 2 were 1. LIAIHA 2. H2O* 1. Mg 2. CO2 3. Ho 4. CH CH2CH2CH2OH, H2SO4(catalytic amount) 1. Na2Cr2O7. H2SO4 H2O 2. Soch 3. (CH3CH2CH2) Culi IO 1. SOCI 2. CH.CH OH o OH
4. Synthesis Reactions. Draw the feature product of the following reactions. (8 x 3 pts) 1. Mg Ph Br 2. CO2 3. H a "NH2 Ph 1. NaOH, CI 2. LAIH b. CHỊCH NHA NaBHgCN, H+ Ph C. Br (excess) NH d NaOH H HO OH H CH e. 1. NaOH H2O NH 2. H+ o= 1. NaOH H2O 2. SOCI N(CH3)2 3 HO
ICA 11-19-2019 Carboxylic Acids Please complete the following assignment on your own paper. 1. Name the following using IUPAC Naming. Name and Rank the following compounds as Most Acidic, Middle and Least Acid 0 он со он Cr-
Do all work on this paper. 1. The compound below on the left has a much higher melting point than its isomer on the right. Explain. (4 points) Tronohon o llottobu 2. Strong acids always protonate amide oxygens and never protonate amide nitrogens. Provide two reasons that explain this fact (4 points). 3. Draw the complete mechanism of the reaction below and indicate the location of "O in the product. (6 points). CH, + 1 equivalent of KOH in water...
25 Predict the product in the following examples, showing stereochemistry when appropriate (21) #) Write a structural formula for the principal organic products) of each of the following reactions 1) Na MON 2) H,09 CH.CH -OCH гон i 1 NaCN, DMSO 2) H 3) H,O', heat -CO,H HNO H2SO4 -NO; Br FeBry -NO, CHOCI AICI COM heat cl Febry 1) KOCH, 2) H30 b) Write a structural formula for A-C -EN 1260 1) CHI CHA Mp4r, Et (0) OH WNO...