maddib7426 maddib7426

03-12-2019
Chemistry

contestada

Draw a structure for the product of nucleophilic substitution obtained on solvolysis of tert−butyl bromide in methanol, and arrange the correct mechanism for its formation. Be sure to answer all parts.

Respuesta :

jescaherga jescaherga

04-12-2019

Answer:

2-methoxy-2-methylpropane

Explanation:

The first step for this reaction is the carbocation formation. In this step, a tertiary carbocation is formed. Also, we will have a good leaving group so bromide will be formed. Then the methanol acts as a nucleophile and attacks the carbocation. Next, a positive charge is generated upon the oxygen, this charge can be removed when the hydrogen leaves the molecule as [tex]H^+[/tex]. (See figure)

Ver imagen jescaherga

Answer Link

Otras preguntas

thA sum of Rs. 700 grows by 1/20 of itself every year. At what time would it amout to Rs.1050? a) 8 yearsb) 10 yearsc) 12 years d) 15 years

Express the product of 3x^2 - 4x +6 and x-2 in standard form.

Two of the lights at the local stadium are flickering. They both just flickered at the same time. One of the lights flickers every 7 seconds and the other light

ANP is a hormone that causes:_________ a. constriction of the afferent arterioles and inhibition of renin release. b. dilation of the afferent arterioles and in

Can you please Solve for x

Hume argues that these things are fundamental to our daily experience that no sane person could possibly doubt them, yet they are completely without justificati

Jake remembers his grandfather telling him about going to work at 16 years of age in the coal mines of southern Illinois. In order to get the job, he had to agr

what does grit mean in psychology

Explain how to solve 5x2-3x = 25 by completing the square. What are the solutions?

What is the complete ionic equation for this reaction? 2KOH(aq) + H2SO4(aq) → 2H20(1) + K2SO4(aq) O A. 2K+ + OH + H2SO4 → OH + 2H+ + K2SO4 B. OH + 2H+ + 2H20()