The reaction of Cl2/H2O with 1-methylcyclohexene gives which product as a racemate? Please explain or show how.
The reaction of Cl2/H2O with 1-methylcyclohexene gives which product as a racemate? Please explain or show...
Please show your work
The reaction of 1,3-pentadiene with hydrogen chloride (HCI) gives the product shown below (as a racemate). However, the reaction with deuterium chloride (DCI) produces two products, A and B (also as racemates), and the ratio of these is temperature dependent. Which product, A or B is favored at low temperatures (0°C) and What happens to the ratio at higher temperatures (40°C)? Explain these in terms of kinetic vs thermodynamic control. (20 points d. How might you...
1. What is the major product for the following
reaction?
2. What is the major product for the following
reaction?
3.
4. Which reagent or test could be used to distinguish between
3-methyl-2-octene and 3-methyloctane?
Ethanol
Br2/CCl4
Sodium hydroxide aqueous solution
Two of these choices.
All of these choices.
5. Which of the following reagents give the highest yield for
conversion of 2-bromopentane to 1-pentene?
KOH/H2O
KOH/CH3OH
(CH3)3COK/(CH3)3COH
CH3ONa/CH3OH
CH3CH2ONa/CH3CH2OH
6.
What is the major product for the following reaction?...
What is the mechanism for this reaction? Please draw out the
hydrogens and electrons included in this process
0 N° N-bromosuccinimide (NBS) ~ , Br OH or CH, H2O, THE "CH3 T''Br CH3 1- methylcyclohexene Markovnikov product anti-Markovnikov product
1) In the reaction of Cl2 with ethane and UV light, which of the following reactions would be a chain termination event(s)? 1) CI: + CH3-CH3 - CH3-CH2-CI+H II) CI+ CH3-CH3 CH3-H2C + HCI III) Cl. + CH3-H2C-CH3-CH2-CI IV) Cl2 + CH3-H2C - CH3-CH2-CI+CI- V) Cl2 + UV light -CI+CI: A) reaction V B) reactions I and IV C) reactions III and IV D) reactions I and II E) reaction III 2) Given the chlorination of acetone shown below, choose...
1) In the reaction of Cl2 with ethane and UV light, which of the following reactions would be a chain termination event(s)? 1) Cl. + CH3-CH3 CH3-CH2-CI+H. II) CI+ CH3-CH3 CH3-H2C + HCI III) Cl. + CH3-H2C: CH3-CH2-CI IV)Cl2 + CH3-H2C CH3-CH2-CI+ CI: V) Cl2 + UV light - CI+CI- A) reaction V B) reactions I and IV C) reactions III and IV D) reactions I and II E) reaction III 2) Given the chlorination of acetone shown below.choose the...
1. starting with 1-methylcyclohexene show synthesis of 2-methylcyclohexanone 2. show the major product for the reaction between Br2/FeBr3 and benzene. Additionally outline a detailed mechanism for the formation of the product.
Can you please draw it and explain
Which of the following compounds is the product of the reaction shown that displays retention of configuration compared to the starting material? H2O Sni a . H d. HO, b. Br CH3 H H3C он OH c. CH3
What alcohol would be used as the starting material to obtain 1-methylcyclohexene as a product in an E1 elimination reaction when using sulfuric acid as a catalyst and H2O as the solvent to pull the hydrogen from the carbocation. Please explain why that alcohol would be used.
PLEASE ASAP ANSWER
Predict the major product for the following reactions
CH=CH2 CH3 Cl2 H2O az CCA CH3 H2 Pd CH3 нс H СНаз, KOH H CH3 1.0, CH2013 2Zn, HOẶC
Provide the structure of the organic product(s), which result
in the reaction below. (Hint: this is a substitution product)
PLEASE EXPLAIN!
N . (4 pts) Provide the structure of the organic product(s), which result in the reaction below. (Hint: this is a substitution product) CH3 CI CH,CH OH CH + CH₃ CH₂ ce