The bromine addition to ethene is an atom-economic reaction that means it is a reaction where there are no byproducts, only one type of product is formed and thus this reaction will also yield a dibromo product since Br2 adds to the ethene double bond.
Homolytic cleavage of the bromine molecule will generate two bromine radicals and thus these radicals will activate the double bond and will add to it.
Thus the first step is the radical addition to the double bond and then the monobromine radical intermediate is formed and then the second bromine radical adds to the intermediate to give a dibromo product as shown above.
Really confused about this problem.Please tell me the answer as specific as possible!Thanks! The following addition...
Really confused about this problem.Please tell me the answer as specific as possible!Thanks! The following addition reaction will proceed when bromine forms two radicals via homolytic cleavage. The radicals then react with ethene to form which product? HH C=C + Brz
Really confused about this problem.Please tell me the answer as specific as possible!Thanks! What is the carbon chain product of the elimination reaction beginning with the reactant shown below? Br Hint: the eliminated product is HBr. What is left? НС-CH H2C=CH2 CHBr CHBr CH2Br-CH2Br
Can you explain how to get this answer? I’m confused on how to get this specific lewis structure from the information given and where the C2H4 would go in the final product The following addition reaction will proceed when bromine forms two radicals via homolytic cleavage. The radicals then react with ethene to form which product? HH C= C + 1 H Bra , Br
Really confused about this problem.Please tell me the answer as specific as possible!Thanks! 1. An employee of a firm has a job where the employee can easily adjust the number of hours they work for the employer per year. The employee is currently paid $40 per hour and will work 2000 hours in 2018. The employer had a good year in 2018 and is considering two changes in the employee's compensation for 2019. a) Suppose the employer decides to raise...
Really confused about this problem.Why it is D?Please tell me the answer as specific as possible!Thanks! Observe the structure below and answer the next two questions. НО. On this same structure, which group will be removed in the condensation mechanism? rect Answer OD В
Really really confused about this problem.Please tell me the answer as specific as possible!Thanks! 2. Answer the following based on the table below which is the cost of one of many identical firms in a perfectly competitive market. Assume the good can only be produced in whole quantities (ie q = 4.7 not possible). All given numbers in the table are exact. (No rounding). Also assume that the amount of capital the firm is stuck with in the SR to...
For this question, I really confused about why a=this thing. Also, could you please tell me the specific steps of the thing that I highlighted in a red pen? I really don’t know how to use math to deal with it. Finally could you tell me how to calculate Var(3X1),VarX2 and Cov(3X1-X2)? Thanks! Will rate:) 각 --Ye a where aa Chec 각 --Ye a where aa Chec
Answer the following questions about radical halogenation QUESTION 1 Performing allylic bromination of an asymmetric alkene produces two regiochemical outcomes due to resonance, and two conformations (R) and (S) for each chirality center produced. This is further complicated if you make the mistake of using Br2 as your source of bromine radicals, as the addition reaction producing alkyl dibromides competes with the allylic bromination. Br2, hv ??? Categorize each of the compounds shown below as an [A] allylic bromination product,...
3.Help, this got me really confused. ORGANIC CHEMISTRY 353 UPPER LEVEL. THANKS 1. (4 pts) Arrange the following compounds in order of increasing acidity (4 = most acidic): HH Meo OME 2. (4 pts.) Arrange the following in order of increasing electrophilic aromatic substitution reactivity (4 = most reactive): Br OMe 3. (4 pts.) Briefly describe why alkenes undergo addition and aromatic compounds undergo substitution. 4. (5 pts. Provide an example of an EAS reaction creates an arene that is...
4.help, this got me really confused. ORGANIC CHEMISTRY 353 UPPER LEVEL. THANKS 1. (4 pts) Arrange the following compounds in order of increasing acidity (4 = most acidic): HH Meo OME 2. (4 pts.) Arrange the following in order of increasing electrophilic aromatic substitution reactivity (4 = most reactive): Br OMe 3. (4 pts.) Briefly describe why alkenes undergo addition and aromatic compounds undergo substitution. 4. (5 pts. Provide an example of an EAS reaction creates an arene that is...