Write the mechanism for the formation of the t-butyl cation from t-butanol and H2SO4
The mechanism for the formation of t-butyl cation is given in the above fig.
Write the mechanism for the formation of the t-butyl cation from t-butanol and H2SO4
H2SO4 (cat) OH n-butanol HO propionic acid homoly od 10.my mol no H₂O n-butyl propionate cal concenteNucleophilie gewl substiti Diabanidaataifianti 3. Answer the following questions: a. For only the ester you are making, please draw a detailed electron-pushing mechanism to show the formation of the compound. There are many resources available to you on the web, etc) for the mechanism of the Fischer esterification reaction. latest some of one of obol whichever one will be using to
Butyl Bromide Assignment: Provide a reasonable curved arrow mechanism for the formation of the following side reaction. H2SO4 OH osogh
Write stepwise mechanisms for thr formation of each product. H2SO4, H20 tert-Butylbromide + tert-Butylchloride tert-Butanol ΝH4Br, ΝΗ,Cl
1. Write a mechanism for adding the first t-butyl substituent to the ring. include a teo step electrophile formation and its two-step displacement of an H 2. Draw the structures of an alkene and an alcohol that coukd have been used instead of t-butyl alcohol to form 1,4-di-t-butyl-2,5-dimethoxybenzene 3. starting with benzene, an alcohol, an inorganic acids, show how to synthesize TNT o LH C(CH₃)₂ а (сн.). Сон OCH3 OCH3 Octs с (сн.) си, 0043 CH3CH2CCH І биз 1 Он
Create a step by step mechanism for 1-butanol reacting with acetic acid to form butyl acetate. Under what circumstances would the equilibrium lie to the right? To the left?
Write a detailed reaction mechanism for the reaction between 2-methyl-2-butanol and concentrated HCl. If 2-methyl-2-butanol was treated with concentrated H2SO4 instead of concentrated HCl, what product would predominate?
show the mechanism for the formation of the product starting from the hemiacetal given H2SO4 OHے HO ОН 0 OH hemiacetal
Answer the following problem: Show the mechanism for making tert-butyl carbocation from tert-butyl alcohol in the presence of sulfuric acid or phosphoric acid, as catalyst. Alcohols ------[H2SO4 ]----->R+
Help a) Draw a complete mechanism showing how t-butanol is first converted into an electrophile and then how the electrophile is attached to the aromatic ring. b) What is meant by electron donating and electron withdrawing groups on an aromatic ring? Is the methoxy group an EWG or EDG? Is a t-butyl group an EWG or EDG? c) Two equivalents of t-butanol are used in this reaction. What is the likely problem if only one equivalent of t-butanol is used?...
is my synthesis of butanol from acetic acid done correctly? having issues trying to synthesis butyl acetate from acetic acid :/ но acetic + butanol = butyl acetate acid ОН OTSCI, pydrine t-Book Pt THO OH Br, ROOR k Bu ok но бHBr 2002 4 - Bu Ok но Ал 10 40