Draw the major products for the following reaction 1) O3, CH2Cl2,-78 °C 2) Zn, H20 or HOAc
Predict all possible products with stereochemistry if applicable. 1.03 2. Zn, AcOH H2, 25 °C 2. W Lindlar's Catalyst 1. Bre, CCIA 2. excess NaNH, NH3(1) 3. H30+ 3. 1 % Pd(PPh34 Š a le in reprehen 4. 100 °C 1. Na, NH3 (1) 2. H2O
Diels-Alder CN Reaction CN diene dienophile D. 1. 03, -78°C "H H' 2. Zn/H2O 4. Circle all aromatic compounds: (2 points)
Draw the products formed when the following alkene is treated with O3 followed by Zn, H2O. Be sure to answer all parts.
Draw the products formed when the following alkene is treated with O3 followed by Zn, H2O. Click the draw structure button to launch the drawing utility.
What stereoisomers are obtained from the following reactions? (a) 1-butene + H2O/H3O+ (b) (Z)-3-heptene + Br2 (c) cyclohexene + HBr (d) (E)-3-hexene + Br2
2. Predict the products for the following reactions of oxidation: 1. O3, DCM, -78°C 2. DMS 1. KMnO4, OH, heat KMnO4, OH. cold 2. H3O+ KMnO4, OH, heat Predict the mechanism for the reaction of ozonolysis and name all the intermediates:
1) What is the IUPAC name for the following compound? A) 6-Ethyl-6-heptene C) 2-Ethyl-1-heptene B) 2-Ethyl-1-octene D) 6-Ethyl-1-heptene 2) Label each C-C double bond in Kavain, a naturally occurring relaxant, as Eor Z. CH5 Kavain A) I = E and II = E CI= Z and II = E B) I = Z and II = Z D) I = E and II = Z 3) Which of the following statements about alkenes is not true? A) They are less...
Observe the reaction of eugenol with ozone. 1. O3, CH3OH (-78 degrees C) 2. (CH3)2S A. Draw the expected product of the ozonolysis reaction in the box provided B. What changes in the IR do you expect the product to have that is not seen in the starting material? Be sure to give estimate cm^-1 that you would observe
Give an IUPAC name for the following compound: (E)-4-ethyl-3-methyl-2-hexene (E)-3-ethyl-4-methyl-2-heptene (Z)-3-ethyl-5-methyl-2-heptene (Z)-3-ethyl-4-methyl-2-heptene (E)-3-ethyl-4-methyl-2-hexene (E)-3-ethyl-5-methyl-2-heptene (2)-4-ethyl-3-methyl-2-hexene (2)-3-ethyl-4-methyl-2-hexene (Z)-3-ethyl-5-methyl-3-heptene (E)-3-ethyl-5-methyl-3-heptene