7. Draw a Newman projection of the reactive conformation of the starting material Draw the product of the reaction,...
8. Consider the reaction below: a. Draw a Newman projection of the reactive conformation of the starting material. b. Draw a mechanism of the reaction below; draw arrows on the drawing c. Draw the transition state for this reaction use to show partial bonds) d. Draw the product of the reaction, clearly indicating stercochemistry. Ph-phenyl. -CH, H .CH KOH BECH.CH
Draw the product of the following E2 reaction. Fill in the Newman projection of the REACTIVE conformation looking down the direction of the arrow shown. Nah THF CH3
Draw a Newman projection of the anti conformation of 1, 2-dichloroethane. Draw a Newman projection of the gauche conformation of 1, 2-dichloroethane. Draw the Newman eclipsed projection for 1, 2-dichloroethane. Why do you think this conformation, as indicated in in the explanation, does not "exist"?
Which Newman projection represents the reactive conformation when the following alkyl chloride undergoes an E2 reaction to form the Zaitsev product. Ph CH3 CH3 A) ClytyH B) Hyycc) CITYH H3CH PhTH HYPh CH3 CH3 Hc CH3 O Type here to search
7. Consider the reaction below to answer the following question(s). CH H3C-c-c13;0 CH7 HC H3C-C-OH + C=CH, H2C ethanol CH CH3 The substrate in the reaction is: (1 pt) Compound B is the product of mechanism (1 pt) Compound C is the product of mechanism (1 pt) Write the complete reaction mechanism for the formation of Compound C in this reaction. (2 pts) Final Exam- Part 11 (40 pts) Dr. Indika Galpothdeniya 8. Consider the reaction below to answer the...
Conformations of Alkanes and Cycloalkanes 1) Draw a Newman projection of the anni conformation of 1.2-dichloroethane che conformation of 1.2-dichloroethane 2) Draw a Newman projection of the 5) Sight along the C2-C3 bond of 2-methylbutane and draw each of the staggered conformations 4) Arrange the following conformations from lowest to highest energy. CH CH 5) Circle the Most stable conformation of the molecule shown below. н сн, YI 6) Circle the Most stable conformation of the molecule shown below.
Stereospecificity of E2 reactions. Draw out the newman projection in an antiperiplanar conformation needed for E2 reaction and E2 product.
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...
5. Provide the mechanism for the reaction shown below. Provide a Newman projection showing the proper orientation of the molecule for the intermediate formed prior to the rate-determining step. Stereochemistry MUST be correct.(7 points) H I ?? KOH CH3CH2 H CH3CH2 CH3 Mechanism: Newman Projection
Consider the reaction below and answer the following Consider the reaction below to answer the following questions. A. write the product that return true the indicated in the b. Draw a Newman projection of the reactive conformation of the starting material.