Using a piece of paper, draw all the possible monochlorination products that could possibly be formed upon radical chlorination of 2-methylpentane. Highlight the product you believe would be formed in greatest quantity.
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Using a piece of paper, draw all the possible monochlorination products that could possibly be formed...
draw all the possible monochlorination products that could possibly be formed upon radical chlorination of 2-methylpentane. Highlight the product you believe would be formed in greatest quantity. **i was able to draw 6, but i feel they may be wrong - 3-chloro-2-methylpentane, 2-chloro-4-methylpentane, 1-chloro-4-methyl, 2,3,3-dimethylchloropentane, 2,2-chloromethylpentane, 2-chloromethylpentane**
aDraw all of the monochlorination productsthat you might obtain from the free-radical chlorination of 3-methylpentane. products that you might obtain from the free-radical chlorination of 3-methylpentane . You do not have to consider stereochemistry. Draw one structure per sketcher. Add additional sketchers using the drop-down menu in the bottom right corner .Separate gn from the drop-down menu multiple products using the +si
please help 13. The reaction of 3-methyl-1-phenylbutane with chlorine yields four different monochlorination products via a free radical mechanism. The experimental distribution of these products is given below. Use this information to determine the relative reactivity of the primary, secondary, tertiary and secondary benzylic hydrogens under these reaction conditions. SHOW ALL WORK!!! on a ou on oso ona 66.27% 12.54% 11.01% 10.18% 14. The free radical reaction of chlorine with 1,3-dimethyl cyclohexane yields five different monochlorination products. Draw the structure...
Be sure to answer all parts. What products are formed from monochlorination of (2R)-2-bromobutane at Cl and C4? Draw the products using skeletal structures. draw structure ... draw structure ... (reaction at C-1) (reaction at C-4)
Draw all possible monochlorinated products you'd expect upon treating 2-methylbutane with Cl2 and irradiated with UV light. Draw all possible monochlorinated products you'd expect upon treating cyclohexane with Cl2 and irradiated with UV light. Predict the product(s) you'd expect when the following molecule is treated with NBS and irradiated with UV light? Draw the allylic radical intermediates you would expect to form as intermediates in the following reaction Br NBS + hv Br Provide the product you'd expect from the...
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?
1)Draw all alkene prodcuts that could form 2) Circle the major alkene product expected 3) Draw a complete arrow pushing mechanism how the major product is formed. (Show all srrows, intermediate structures, formal charges) 2. (19pts) The alcohol dehydration product below is of the El type elimination. (i) Draw all of the alkene products that could possibly form. (ii) Circle the major alkene product expected. (ii) Draw a complete curved arrow-pushing mechanism illustrating how the major product is formed. Be...
1) Consider the free radical monochlorination of 3-methylpentane and answer the following: a) How many products (including stereoisomers) are formed? _______ b) How many are chiral? ________ c) Would the major product of free radical bromination possess a chiral carbon? Yes or No 2) Which of the following functional groups can be generated in one step via SN2 or SN1 reaction? (Enter all that apply) a) Aldehyde b) Alcohol c) Alkene d) Alkyne e) Amine f) Carboxylic Acid g) Ester...
1. Draw all the products that would have resulted if 2-chlorobutane were used for a radical chlorination