1 This Question Is Similar To Textbook Worked Example 10 1 And Problems 10 5 To 10 7 The Reaction Of 2 Methylbut 1 Ene 1 (29.75 KiB) Viewed 43 times
1 This Question Is Similar To Textbook Worked Example 10 1 And Problems 10 5 To 10 7 The Reaction Of 2 Methylbut 1 Ene 2 (24.21 KiB) Viewed 43 times
1. This question is similar to textbook worked example 10-1 and problems 10-5 to 10-7. The reaction of 2-methylbut-1-ene with N-bromosuccinimide may produce a mixture of products. CH₂ NBS hv, CCIA (1) Identify the allylic positions of the reactant (2) Draw all possible allylic radicals that may form during the reaction (Br- radical abstracts an allylic hydrogen atom) (3) Draw resonance structures of each of the allylic radical (4) Draw the possible products (by adding Br- to carbon with an unpaired electron)
2. Practice textbook problem 10-11 first before working on this question. How would you carry out the following transformations using an organocopper coupling reaction? More than one step is required in each case. CH₂CH₂CH₂Cl CH3CH₂CH₂CH₂CH₂CH₂ CH₂CH=CH₂ CH3CH₂CH₂CH₂CH₂CH3
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