Question

Use Newman projections to show the mechanism of the addition of bromine to trans- and cis-stilbene.

Use Newman projections to show the mechanism of the addition of bromine to trans- and cis-stilbene.

Homework Answers

Answer #1

Answer: According to question the mechanism of addition of bromine is based on the addition reaction and it is shown as :

Hence it is all about the given question . thank you :)

Know the answer?
Your Answer:

Post as a guest

Your Name:

What's your source?

Earn Coins

Coins can be redeemed for fabulous gifts.

Not the answer you're looking for?
Ask your own homework help question
Similar Questions
What is the stereochemistry of the bromine addition to trans-stilbene? Explain using your experimental evidence.
What is the stereochemistry of the bromine addition to trans-stilbene? Explain using your experimental evidence.
Lab 6: Electrophilic Addition Reactions: Bromination of cis- and trans-stilbene My product was cis-stilbene, 1,2-dibromo-1,2-diphenylethane 1....
Lab 6: Electrophilic Addition Reactions: Bromination of cis- and trans-stilbene My product was cis-stilbene, 1,2-dibromo-1,2-diphenylethane 1. Following the reaction, the reaction mixture was diluted with water and placed in an ice-water bath. Why? (5 Pts total) 2.Calculate the theoretical and percent yields of your bromination reaction. Assume that cis or trans stilbene is the limiting reagent. Show all steps of your calculations. (5 Pts) 3. Draw the bromination mechanism that your reaction proceeded through for Lab 6. Remember to assign...
Why is the bromination of trans and cis-stilbene with pyridinium tribromide not carbocation intermediate? I know...
Why is the bromination of trans and cis-stilbene with pyridinium tribromide not carbocation intermediate? I know that it is bromonium ion mechanism, I just do not know how we know that it isn’t carbocation intermediate mechanism.
Suppose in the reaction preparation of Diphenylacetylene you start with cis-stilbene instead of trans-stilbene, would you...
Suppose in the reaction preparation of Diphenylacetylene you start with cis-stilbene instead of trans-stilbene, would you expect the MP of the stilbene dibromide produced be the same as the one obtained from trans stilbene? Why and why not?
When ethanolic silver nitrate is added, why does trans-stilbene not form a precipitate while cis-stilbene does...
When ethanolic silver nitrate is added, why does trans-stilbene not form a precipitate while cis-stilbene does form a precipiate. Explain how there different structures influence this observation.
explain any differences or similarities in the stereochemistry of the bromine addition reactions of trans-cinnamic acid...
explain any differences or similarities in the stereochemistry of the bromine addition reactions of trans-cinnamic acid and trans-anethole.
Draw the mechanism for the elimination of the product from Question #2 (written below) using KOH...
Draw the mechanism for the elimination of the product from Question #2 (written below) using KOH and heat. The first elimination follows a classical E2 mechanism and the product is an alkene with the phenyl groups in a cis configuration. Since the bromine and hydrogen are not in an anti-coplanar arrangement, the second elimination cannot proceed through an E2 mechanism. Instead it is said to proceed through an E1cB mechanism. Question 2 for reference: Draw the mechanism for the bromination...
a. Based on the stereochemistry of the addition of bromine to trans-cinnamic acid, write the structure...
a. Based on the stereochemistry of the addition of bromine to trans-cinnamic acid, write the structure of the product(s) that will form when bromine reacts with (Z)-2-hexene. b. Assume that you carried out separate reactions of bromine with (E)-2-pentene and (Z)-2- pentene. After isolating, purifying and determining the melting point of the product from each reaction, you found that the melting points were significantly different. Explain why. c. Why did you dry your product in the oven before taking its...
how can i use group theory to determine if I have cis or trans Mo(CO)4(PPh3)2. Please...
how can i use group theory to determine if I have cis or trans Mo(CO)4(PPh3)2. Please explain because I have to give a full explanation
   1. Show all the products obtained from the ozonolysis of the following alkenes. a.     1-hexene...
   1. Show all the products obtained from the ozonolysis of the following alkenes. a.     1-hexene b.         2-methyl-2-pentene c.         cis-3-methyl-3-hexene d.         2,3-dimethylbut-2-ene e.        2,3-dimethylpent-2-ene 2. Stating whether the reaction between (+)-3-iodo-3-methylheptane and sodium ethoxide would follow SN1 or SN2 substitution mechanism, show the complete mechanism of the reaction emphasizing stereochemical changes observed, if any. 3. Showing the detailed stereochemistry, give the mechanism and products of epoxidation (with m-CPBA) and borane (with BH3-THF) addition reactions on cis- and...