e the mechanism for the following reaction 3,4-dimethyl-2-pentene NaBHa (OAc)2, HOAo 2H20 e the mechanism for the following reaction 3,4-dimethyl-2-pentene NaBHa (OAc)2, HOAo 2H20
"provide products and mechanisms for (z)-3,4-dimethyl-2-pentene reaction with Br2 in H2o including stereochemisty"
1. Give the complete reaction mechanism for the acid catalyzed hydration if 3,4-dimethyl-1-butene showing all intermediates and products. (10 pts).
Using curved arrows to designate the flow of electrons, provide a detailed stepwise mechanism for the reaction of 3,4-dimethyl-3-pentanol as a starting material, with 3,4 -dimethyl-3-pentene (45% yield) and 3,4-dimethyl-3-chloropentane (55%) as the products.
Please answer thoroughly! 1. Hg(OAc)2 2. NaBHA ? 11. 1.5% Which type of reaction took place? The reason for your selection in the question above Pertinent mechanistic details OH ? 12. 1.5% Which type of reaction took place? The reason for your selection in the question above Pertinent mechanistic details OH ОН ? ☺ + 13. 1% Which type of reaction took place? _The reason for your selection in the question above Brci 14. 4% Which type of reaction took...
What is the major product is this reaction sequence? Cl2, hv NaOET Hg(OAC)2, H20 NaBHA Br2 EtOH FeBrz OH OH OH BI Br А B с D СА OB Сс D What is the effect of halving the amount of ethanol for this reaction? Br. EtOH Δ A. The reaction rate decreases by half B. The reaction rate quadruples C. The reaction rate doubles D. The reaction rate stays the same
IZDI 4) What is the major organic product of the following reaction? NaOCH_CH: A) 2,3-dimethyl-2-hexene B) (E)-2,3-dimethyl-3-hexene C) (2)-2,3-dimethyl-3-hexene D) 2-isopropyl-1-pentene E) 2,3-dimethyl-1-hexene ila nf the following statements correctly describe(s) E1 reactions of
1. Hg(OAc)2, H20 2. NaBHA CH3 M HC CHE нас Acid-catalyzed addition of water to an alkene yields an alcohol with Markovnikov regiochemistry. The electrophilic H adds to the sp carbon with the most hydrogens to yield the most stable carbocation intermediate, which then adds water to give the product alcohol. Because a carbocation intermediate is formed, rearrangements can occur prior to the addition of water To avoid the possibility of rearrangement and still give a Markovnikov alcohol, alkenes can...
Suggest a mechanism for the following electrophilic addition reaction OH 1) Hg(OAC)2, anhydrous THE 2) NaBH, then hydrolysis
Which of the following compounds would react the slowest with HBr A) 2,3-dimethyl-2-pentene B) 2-methylpropene C) 3-methyl-1-butene D) 2-methyl-1-butene E) 2-methyl-2-butene
Draw the structure of the major organic product of the following reaction. CH3 CH3CH 1. Hg(OAC)2, H2O O- CH3 2. NaBH4 You do not have to consider stereochemistry. In cases where there is more than one answer, just draw one. - @./ 7. OOO. IF ChemDoodle Draw structural formulas for all alkenes that could be used to prepare the alcohol shown below by oxymercuration. 2 1. Hg(OAc)2, H2O 2. NaBHA ОН (CH3)2CHCCH(CH3)2 CH3 You do not have to consider stereochemistry....