5. Upon reaction of 3-methyl-4-phenyl-2-heptanol with concentrated aqueous hydrochloric acid, the major product 4-chloro-3-methyl-4-phenylheptane was found....
5. Upon reaction of 3-methyl-4-phenyl-2-heptanol with concentrated aqueous hydrochloric acid, the major product 4-chloro-3-methyl-4-phenylheptane was found. Show the mechanism for this reaction.
Just Answer Question 5 Synthesis of 2-chloro-2-methylbutane (literature version) Concentrated aqueous hydrochloric acid (HCI, 3.3 equivalents) was slowly added to 2-methyl-2-butanol (1.0 equivalents) in a 100 mL round bottom flask with stirring. The reaction was stirred for 15 minutes at room temperature. Upon completion, the reaction mixture was transferred to a 60 mL separatory funnel and the aqueous layer was removed. The organic layer (i.e. the product) was successively washed with: (1) saturated aqueous NaCl (brine), (2) saturated aqueous NaHCO,...
A student was planning to synthesize 2-chloro-3-methylbutane from 3-methyl-2-butanol using concentrated HCl, similar to the reaction you did. When the experiment was carried out, the product isolated was 2-chloro-2-methylbutane. Explain these results by showing a plausible mechanism for the formation of 2-chloro-2-methylbutane under these reaction conditions. (Hint: it is an SN1 reaction, but think about what can happen to the carbocation intermediate that we learned about in lecture to cause that product to form.)
4-chloro-2-methyl-2-pentene reacts with acetic acid (solvent), two substitution products are urmea, with the rearranged product predominating as shown in the diagram that follows. When small amounts of acetate ion are added to the reaction mixture, no increase in the rate is observed. Propose a mechanism that accounts for these results. Explain clearly why two products are formed (5 points) Minor Major
what is the major product? What is the major product of the following reaction? OH 2 de ore 1. SOCI2 2. (CH3)2Culi Product Produc methyl phenyl ketone 1-phenylethanol 2-phenyl-2-propanol 1-chloro-1-phenylethane
1.The main product of the reaction between p-cresol and Br2 / FeBr3 is: 3-Bromo-4-methyl phenol 2-Bromo-4-methyl phenol 2-methyl-4-bromine phenol 3-methyl-4-bromine phenol 2.Which of the following compounds is the least reactive in the nucleophilic substitution with NaOH? 2,4-dinitrochlorobenzene m-nitrochlorobenzene o-nitrochlorobenzene 3,5-dinitrochlorobenzene 3.What is the mechanism (s) for the reaction of 4-bromo-1-nitrobenzene with sodium hydroxide to form 4-nitrophenol? bimolecular nucleophilic substitution (Sn2) aromatic nucleophilic substitution by addition-elimination aromatic nucleophilic substitution by elimination-addition aromatic electrophilic substitution 4.which of the following is the correct...
1. 3-methyl-1-butene on reaction with H-Cl forms two products, namely 2-chloro-3- methylbutane (minor) and 2-chloro-2-methylbutane (major). Illustrate the mechanism for the formation of these two products. Use curved arrows to illustrate electron movement and all intermediates must be shown. 2. 3,3-dimethyl-1-butene on reaction with HBr forms two products, namely 3-bromo-2,2- dimethylbutane (minor) and 2-bromo-2,3-dimethylbutane (major). Illustrate the mechanism for the formation of these two products. Use curved arrows to illustrate electron movement and all intermediates must be shown. 3. Calculate...
#12 of A,B-unsat Addition What is the major organic product expected from the reaction of methyl 3-phenyl-2-propynoate with one mole equivalent of benzylamine followed by a mild acid workup? Select one: a. methyl 3-phenyl-2-propenoate b. methyl 3-(N-benzylamino)-3-phenyl-2-propenoate c. methyl 2-(N-benzylamino)-3-phenylpropanoate d. ethyl 2-(N-benzylamino)-3-phenylpropenoate e. benzyl alcohol
What is the product of the following reaction sequence? MgCH CH2CCH3 Ho O 2-heptanol 2-methyl-3-hexanol O 3-methyl-3-hexanol 3-ethyl-2-pentanol
Do ASAP like you were doing an exam. Thanks. do asap 3. When (S)-4-ethyl hexan-3-ol was treated with concentrated hydrochloric acid the major product formed was 3-chloro-3-ethylhexane. This reaction involved an Sy1 mechanism. (15 pts) b. A minor product of this reaction is the (R/S)-3-chloro-4-ethylhexane. Explain using step by step mechanism why this compound a mixture of isomers? (10 pts) CH3 Нас CI CH3 3-chloro-4-ethylhexane