Post-Lab Questions 1. Give the expected Zaitsev and anti-Zaitsev products in the following reactions. Label the...
organic chemistry II lab help 1-4 plz
Post-Lab Questions 1. Give the products from the following reactions Nabi CHOM Nath CH, OH 2. What key IR and NMR absorptions would allow you to determine that the products from the reactions above have been successfully synthesized? Ignore absorption also found in the reactant 3. Nal, usually reacts slowly or not at all with esters. Therefore, LiAlH, is often needed to reduce esters. Why do you think LiAiH, is more reactive than...
Draw the products of the following reactions. Indicate
stereochemistry where appropriate.
POST-LAB QUESTIONS 1. Draw the product(s) of the following reactions. Indicate stereochemistry wher appropriate: 1. NaBH4 a. NH2 2. H20 1. LiAlH4 b. 2. H20 CO X ama = 10.01
Complete the following with the correct products, label Zaitsev and Hofmann, and explain why the reaction is either regioselective or stereoselective. (6 pts.) D -Br Nahi Complete each of the following reactions by adding the starting material, reaction conditions, or all possible product(s) - label major/minor - Sx2. Sx1, E2 or E1. (33 pts.) (CH3),COK DMF C(CH3) NaOH DMSO CH OH heat Ph H+Br NaOCH, H+CHE Ph DMF SK DMF o (only product)
Post-Lab Questions 1. Give the product for the following reactions. Br2, FeBr3 Cl2, FeCl3 b) 2. What key IR and NMR absorptions would allow you to determine that the product from the first reaction above has been successfully synthesized? Ignore absorptions also found in the reactant.
1. Draw the possible E2 products and circle the Zaitsev
products.
2. Draw a Newman projection for the preferred anti-periplanar
conformation leading to the Zaitsev product.
3. Predict the stereochemistry of the Zaitsev products based on
your Newman projection.
Hi! Can someone help me go through the correct steps? Ignore the
pen marks I made:)
eoh E2 Br 2 1. Draw the possible E2 products and circle the Zaitsev products 2. Draw a Newman projection for the preferred anti-periplanar conformation...
Post Lab questions 1. Complete the following reactions and name the products. CH3 -CH=CH2 + CI + Brz c) CH3 -CH=CH-CH, + HBr - Pt d) CH3 -CH2-CH=CH2 + H 25 °C, I am A Bez 2. Toluene contains a benzene ring with three double bonds in it, but still does not show any signs of undergoing a reaction with bromine solution. Why? 3. Why doesn't cyclohexane decolorize the orange-red color of the bromine or the purple color of KMnO...
Post Lab questions 1. Complete the following reactions and name the products. a) CH3 -CH=CH2 CI + b) + Bry c) CH3 -CH=CH-CH3 + HBE Pt d) CH3 -CH2-CH=CH2 + H 25 °C, 1 atm e) + Brz 2. Toluene contains a benzene ring with three double bonds in it, but still does not show any signs of undergoing a reaction with bromine solution. Why? 3. Why doesn't cyclohexane decolorize the orange-red color of the bromine or the purple color...
Preparation of Diphenylacetylene Post-Lab Questions: de the appropriate reagent(s) and/or product(s) for the following line reactions: HBr 2 equivalents 1) 9-BBN, THE 2) H2O2, -OH
Melathesis Reactions Metathesis Reactions Post Lab For the following reactions, write the formula for the expected products, the observations you made during the experiment, the formula for the product that led to those observations, and net ionic equation. Be sure to write equations that include the physical state (g. 6, s. oraq), the charges on the separated ions, and correct balancing Reactants Formulas of Expected Products Observations Product Responsible for Observations Naci PHNO) РЬСІ, Net Ionic Equation: Na:CO: BaCl2 PbCI:...
Question 13 10 pts Label each of the alkene products below as either (Zaitsev, Hoffman, or neither). 8 H_SO OH heat Compound A: Select Compound B: [Select] Compound C: [Select