5.(2) Draw the product of treating each alcohol with is 1- hex and (in 2-hexanol (in...
Predict the product for the following reaction. 1-hexanol PCC CH2Cl2 A hexanal B) 2-chlorohexane C hexanoic acid D 1-hexanol E 2-hexanone
6. Draw the product for each step of the reaction. (#points each) 1. Phli 2. H30* TBAF Br HOOH TSOH Dean-Stark app Page 5 of 10 Name: PCC 1. (CH3)2Culi 2. H30* 1. PhMgBr 2. H30* (d) PPh light n-Buli Name: Page 6 of 10
4. Draw the products of the complete oxidation of 1-hexanol. (Name any product you knogw to.) 5. Draw the reaction of 3-heptanone with excess 1-propanol in the presence of acid.
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):
Homework Problems 8.1 Draw the structural formula for each of the following: a. 5-chloro-4-methyl-2-hexanol b. 2,3-dimethylcyclopentanol c. 5,5-diethyl-1-heptanol d. 2-ethyl-4-isopropylcyclohexanol e. 4-ethylphenol f. 2-nitrophenol g. cyclopropyl methyl ether h. isopropyl propyl ether 8.2 Give the product for the dehydration of each of the following alcohols. CH-CH2-CH3 a. ОН b. ОН C. OH d. 8.3 What product would result from the oxidation of each of the following alcohols? Write the chemical equations. a. 2-butanol b. 2-methyl-2-pentanol c. cyclohexanol d. 3-ethylcyclopentanol Name...
First, clearly draw and label the starting compound given by name below (3,4-dimethyl-1-hexanol). Next, predict the product for each of the reaction steps below (A, B, and C), and then draw the final product D. Very important: Be sure to show your work for each step, including mechanisms for steps covered in class. 1. 3,4-dimethyl-1-hexanol soch H Mg/ether 3,4-dimethyl-1-hexanol SOCI2 pyridine A a Malther B W B C 2. H30+ Croz H2SO4/H20
(1) Show the product of each alcohol oxidation reaction below: OH Croz H30", acetone PCC CH2Cl2 OH Cr₂O, OH H.SO 4, H2O PCC HO CH2Cl2 Nag H2S04, H20 (2) Propose an efficient synthesis for each transformation below mocow OH НО? .name مل.بلو HO / تم.-م" (E) Ph amion e no (F) OMe
Signature (25 points) Draw the structure of the expected major organic product for each of the following five (5) questions Specify stereochemistry clearly, if relevant. PCC a) NaOCH b.) dil. aq. HCI
please write neatly
1. Draw the products of each of the four steps in the designated boxes (5 points per box). step 1 step 2 PCC H_ H step 3 2) H20, HT step 4 NaOCH3 CH3OH Product
Write a mechanism for Butanal, Ethyl alcohol, and potassium hydroxide to form 2-ethyl-hex-2-enal.