4. The transformation of the alkyl chloride shown below into the alcohol can be accomplished in...
4. The transformation of the alkyl chloride shown below into the alcohol can be accomplished in two steps. Show the synthetic scheme to finish the conversion. (1 point) OH
Bonus 3. Give the structures of the two products for addition reaction of HCl to 3-methyl-1-pentene (1 point). Point out which one is the major product, and explain why! (Hint: dont forget carbocation rearrangement) 4. The transformation of the alkyl chloride shown below into the alcohol can be accomplished in two steps. Show the synthetic scheme to finish the conversion. (1 point) Он Br
3. Give the structures of the two products for addition reaction of HCI to 3-methyl-1-pentene (1 point), Point out which one is the major product, and explain why! (Hint: dont forget carbocation rearrangement) 4. The transformation of the alkyl chloride shown below into the alcohol can be accomplished in two steps. Show the synthetic scheme to finish the conversion. (1 point) OH
1. Give the structure of the product(s) for the following addition reactions. Show appropriate stereochemistry if necessary to get the full credits. (5 points) 50% H2SO4 50% H20 1. BH3, THF 2. H2O2/KOH CH3COOH ry condon YY PEO 1. 03 2. Zn/H2O 2. Give the syn or anti addition products for the following addition reactions. Show appropriate stereochemistry if necessary to get the full credits. (5 points total) Hz/Pt 1 point 1 point Hypt DBk Det ook o BryH2O 1....
The following transformation can be easily accomplished under either of the conditions shown. Provide a complete arrow-pushing mechanism for each of these methods to accomplish the transformation (10 points total, 5 points each mechanism). NaOH ОН ОН
For each of the transformations below, provide the reagents necessary. Each transformation can be accomplished in 4 or fewer steps. Be sure to indicate stereochemistry where relevant!
Question 10.16 The following alkyl chloride can be prepared by reaction of the alcohol QR)-2-pentanol with SOcly alkyl chloride, including (R) or (S) stereochemistry, and tell whether the reaction of the alcohol occurs with retention of the same stereochemistry or with a change in stereochemistry ball & stick (t is not necessary to use italics in writing compound names. The answer field is case-sensit Name: Stereochemustry:ーーーーリ Try Another Versio 7 iteen astempts remaining Submit Answer
Complete the reaction scheme below by adding the reagents necessary to accomplish the transformation shown (write your answer in the box provided): [6 pts] он он SMe он Cl 3. Draw the mechanism of the reaction shown below: 15 pts] Me H2SO4 он racemic
2. Complete the transformation shown below. 2. Complete the transformation shown below. (6 pts; no partial point) con ОН LOH -OH (not direct deprotonation) LOH reagent doesn't contain halogen atoms (only product)
2. Complete the transformation shown below. 2. Complete the transformation shown below. (6 pts; no partial point) con ОН LOH -OH (not direct deprotonation) LOH reagent doesn't contain halogen atoms (only product)