mechanism please!
2). i) KOt-Ви Me Me ії) А, о H t-Bu А. о он о t-Bu" Me Me Me t-Bu Me В. D. ОН о Ме. t-Bu. Me t-Bu Me Me
help please with constructing an arrow pushing mechanism for
this reaction!
- T5 он о Сн, нс ОН o-CH,
What will be the product of this reaction? CI H2O CI acetone 요 ОН ОН НО НО. А B о ОА ов ос о There will be no reaction Which of these is the correct mechanism for the substitution of tert-butyl chloride? H Hot Hot H ta - Hot - Но c) toinen Hot Hot OA ос
Work the following mechanism.
10) Work the following mechanism. он о он не c . .. + HO
Please show the complete arrow pushing
mechanism to get both products.
ОН BH3-THE н,О, NaOH, H2O ОН and/or 1-hexene
12.54 please provide a synthesis for the following
transformations:
( a - „О-О-О-О ОН " - ОН 3 -- Со е зE 3 3 3 3 о: 1ттттт HO
major product? thank you!
1. KMnO4 2. SOCI2 3. DIBAL о H ОН ОН CI
Which of the following is a keto-enol tautomeric pair? ОН п он ОН о- Which is the strongest acid? о O ОН CI O ОН F O ОН о ОН Br
Write an arrow formalism mechanism for the following reaction. Explain why 1 is formed, but 2 is not. Он Н,о Н.о OH Be sure to give us two reasons why the OH winds up adjacent to the ring and not on the other carbon of the starting allkene. он H3O* Н.о 2
The 5. Propose a mechanism for the following transformation: (8) Он Н,о