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Can someone answer this question 7. Draw the possible products resulting from addition of 1 equivalent...
7. Draw the possible products resulting from addition of 1 equivalent of HBr to 2-Methyl-1,3-pentadiene. Which would you expect to predominate, and why?
7. Draw the possible products resulting from addition of 1 equivalent of HBr to 2-Methyl-1,3-pentadiene. Which would you expect to predominate, and why?
Show All Steps! 7. Draw the possible products resulting from addition of 1 equivalent of HBr to 2-Methyl-1,3-pentadiene. Which would you expect to predominate, and why? sar
maybe this one is better. I apologize but these are the only pictures I have. Thank you 7. Draw the possible products resulting from noflquale Welch Which would you expect to predominated why 7. Draw the possible products resulting from addition of the Me Which would you expect to predominate, and why?
Draw the kinetic and the thermodynamic addition products formed when one equivalent of HBr reacts with the following compound. (Draw a single product for each. Ignore stereochemical or chiral isomers.) Note: Is this a symmetric or an asymmetric diene? Will it matter which end of the diene you protonate first? Look at this link to see the compound HBr is reacting with: //img.homeworklib.com/questions/ffc52d80-4303-11ea-bc58-936001b91635.png
18 Question (2 points) Draw the major 1.2 and 14-addition products that form as a result of the following reaction between one equivalent each of 2.4-hexadiene and HBr. HBr 1st attempt See Periodic Table O See Hint Part 1 (1 point) Draw the major 1.2-addition product here:
There are three possible products from this experiment: the Markovnikov addition product (1methylcyclohexanol), and the two anti-Markovnikov addition products ((15,2R)-2-methyl- 1cyclohexanol and (1R 2R)-2-methyl-1-cyclohexanol). 1. BH "THE 2. H2O2. NaOH or 3 or 3 OH 1-methyl-1-cyclohexene 1. What is your predicted product? Why? 2. Calculate the theoretical yield. Show calculations including those for the limiting reactant. 0.5 mL of 1-methyl-1-cyclohexene 2.5 mL of 1 M BH, THF solution 0.7 mL of 3 M NaOH followed by 1 mL of 30%...
2. Draw two possible products for the reaction shown below. Are your products formed as a racemic mixture? Which of your two products do you expect to be the major one? Why? 1 equiv. Br2 THF possible product 1 possible product 2 Possible product 1 a racemic mixture? Yes No Possible product 2 a racemic mixture? Yes No Which would be major? Why?
2. Draw two possible products for the reaction shown below. Are your products formed as a racemic mixture? Which of your two products do you expect to be the major one? Why? 1 equiv. VON Br2 THE possible product 1 possible product 2 Possible product la racemic mixture? Yes No Possible product 2 a racemic mixture? Yes No Which would be major? Why?
chapter 9, a,b,c 3) a,b,c 9-31: a,b,c,d c) Chapter 9 1) What products would you expect from the following reactions? a) b) CCH1 HBr- ? c) 2) Arrange the carbocations below in order of increasing stability. Determine primary, se 3) Draw structures corresponding to the following names: a) 5-tert-Butyl-2-methyl-3-octyne b) 3,5-Heptadien-1-yne c) (E)2,2,5,5-Tetramethyl-3-hexene 9-31. Predict the products from reaction of 1-hexyne with the following reagents a. 1 equivalent HBr b. 1 equivalent C12 c. H2, Lindlar catalyst d. 2 equivalent...