3 of 15 A reaction proceeds by the following mechanism: 1. CH4+Cl2-CH3+HCI+CI 2. CH3+Cl2-CH3CI+CI What is the overall reaction? CH4+2Cl2-CH2CI+HCl+2C1- CH4+HCI-CH3CI+H2 OCH4+2Cl2-CH2Cl2+2HCI CH3+C1--CH3C1 4 of 15 Which reaction mechanism is consistent with the overall reaction, 2NO2+F22NO2F? O 1. NO2+F2-NO2F+F 2. NO2+FNO2F O 1. 2NO2-N204 2. N204+F2-NO2F+NO2+F O 1. NO2+F2-NOF+O+F 2. NO2+F=NOF O 1. NO2+F2-NO2F2 2. 2NO2F2-2NO2F+F2
Complete the following reaction: 1-propene (CH2=CH-CH3) + Cl2 = ?
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...
Classify each of the following organic reactions. Substitution Elimination Addition Type of Reaction Reaction CH3-CH2-CH2-CH3 + Cl2 → CH2-CH2-CH2-CH3 + HCI CI CH3-CH=CH-CH3 + Cl2 → CH3-CH-CH-CH3 CICI CH3-CH2-CH-CH3 - CH3-CH2-CH=CH2 + HCI
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...
14) When (R)-2-bromobutane reacts with Cl2/hw, which of the following is true CH3 CH3 H--C1 CH3 CH3 A) Only I is formed. B) Only II is formed. C) I and II are formed in equal amounts. D) I and II are formed in unequal amounts. E) I and II could never form under these conditions. 15) Which of the following compounds is more stable? Explain. -CHb. 16) Give the best product for the reaction. CH CH:CH Br, ight 17) Complete...
Draw the product formed when the compound shown below undergoes a reaction with Bry in CH,Cl2 Interactive 3D display mode CH3
propose a mechanism for the free-radical chlorination of ethane. ch3-ch3 + cl2 +hv ---> ch3-ch2cl + hcl
Part A Draw the product formed when the compound shown below undergoes a reaction with Cl2 in CCI4 Interactive 3D display mode CH3 Draw the molecule on the canvas by choosing buttons from the Tools (for bonds), Atoms, and Advanced Te active by default. Show the appropriate stereochemistry by choosing the dashed or wedged buttons and the
Consider the reaction 2 NO + Cl2 → 2 NOCI A possible mechanism is: Cl2 ⇄ 2 Cl (fast) Cl + NO → NOCl (slow) If this is correct, the rate law will be: A. rate = k [NO]0.5[Cl] B. rate = k [NO]2[Cl2] C. rate = k [NO][Cl2] D. rate = k [NO][Cl]2 E. rate = k [NO][Cl2]0.5