What is the mechanism for 2-methyl-1-butene + ether + HCl to form: 2-methyl-2-chlorobutane
Solution=
In
the first step, double bond take proton from HCl and carbocation is
formed. When it takes proton, both primary and tertiary carbocation
are formed. But tertiary carbocation is most stable. So chloride
attack the tertiary carbocation and the product
2-methyl-2-chlorobutane is formed.
What is the mechanism for 2-methyl-1-butene + ether + HCl to form: 2-methyl-2-chlorobutane
Show the products (major) and mechanism of 3-methyl-butene + HCl. Also, include the hydride shift
Question 34 (Mandatory) (2 points) Name the following molecule CH3 CI Br 1-chloro-2-methyl-4-bromo=2=butene 04-chloro-3-methyl-1-bromo=2=butene 01-bromo-4-chloro-3-methyl-2-butene 04-bromr-1-chloro-2-methyl-2-butene Question 35 (Mandatory) (2 points) Name the following molecule Question 33 (Mandatory) (2 points) Name the following molecule ОН 2-ethoxy-1-ethanol ethyl ethanol ether 2-oxy-1-butanol 1-ethoxy-1-ethanol Question 34 (Mandatory) (2 points) Question 35 (Mandatory) (2 points) Name the following molecule OH p-isopropylmethylphenol 2-isopropyl-5-methylphenol 6-isopropyl-3-methylphenol 2-isopropyl-1-hydroxy-5-methylcyclohexatriene Type here to search о в е Question 36 (Mandatory) (2 points) Name the following molecule 2-methyl-2-oxy-butane 0 1,1-dimethyl ethyl...
Can I-chlorobutane be easily produced from the reaction of 1-butene with HCl and why? (Explain!) (10 pts.) (HINT: You may want to draw out a chemical reaction or two...) 5) Who are there multiple organic or hydrocarbon products produced from the halogenation of alkanes via ultraviolet light? I am grading pretty big on the why part, and it is not only about the number of H's present.....(10 pts.) 6) Using the following monomer, draw the steps and/or mechanism for the...
Relative ranking (#1 - #7) Reason for ranking 1-chlorobutane 1-chloro-2-butene 2-chlorobutane 1-bromobutane 2-chloro-2-methylpropane bromobenzene benzyl chloride (2) What mechanism do you believe will be favored with AgNO3 in ethanol? What order of reactivity do you predict will be observed when each of the alkyl halides in Figure 1is reacted with AgNOs in ethanol? Complete a similar table as in question #1 for these reaction conditions. Write your prediction of the mechanism and the order of reactivity with AGNO3 in ethanol...
(S)-2-chlorobutane was stirred in methanol. The major organic product isolated (97%) was an ether and it was found to be optically inactive. The minor product (3%) was a mixture of three hydrocarbons. Choose the correct statement(s). I. The major organic product was formed via an SN2 reaction. II. The minor products were formed via E1 mechanism. III. The three alkenes formed are 1-butene, cis- and trans-2-butene. Group of answer choices I only I and II only II and III only...
Dehydration of 2-methyl-2-butanol forms a major (2-methyl-2-butene) and a minor (2-methyl-1-butene) organic product. What are the mechanisms for the formation of each when the catalyst used is phosphoric acid?
I just need the potential side reaction that will occur. The
reaction creating the products (2-methyl-1-butene and
2-methyl-2-butene) is between 2-methyl-2-butanol and sulfuric acid.
I already have the arrow pushing mechanism I just do not know what
the potential, undesired side product is. Please show the
mechanism.
Describe and provide a detailed mechanism (use arrow pushing) for the preparation of 2-methyl- 1-butene and 2-methyl-2-butene. 2 pts Provide a potential undesired (side) reaction that can occur during the preparation of the...
A reaction of 2-methyl-2-butene with NBS and heat forms both 1-bromo-2-methyl-2-butene and 3-bromo-2-methyl-1-butene. The reason for the formation of multiple products is: a)Markovnikov and Anti-markovnikov addition b)rearrangement of the radical by hydride shift c)resonance structures of the radical d) dibromination products
Suppose you obtain a mixture of 2-methyl-1-butene (20%) and 2-methyl-2-butene (80%) that equates to 0.2 moles from 0.4 moles of 2-methyl-2-butenel, what is the percent yield of 2-methyl-2-butene? a. 20% b. 40% c. 50% d. 80%
What reagents are required to convert 1-butene to 2-chlorobutane? A) HCI B) CI C) Hz D) H2O, H2SO4