1.
This reaction is called Friedel craft reaction alkylation reaction which involves alkylation of aromatic ring with alkyl halide in presence of strong lewis acid
In the above said example, lewis acid is AlCl3 and benzene is the aromatic compound and dichlormethane is CH2Cl2 is the alkyl halide.
The reaction mechanism is as below.

Q3.
Benzene on reaction with Cl2 in presence of a catalyst gives rise to chlorobenzene. Further on nitration leads to the formation of ortho and para substituted nitro compound because of ortho and para directing nature of chloro group as shown. Metallic hydrogenation reduces the nitro compound to anline. The sequence is shown below.

do both please 2. Write a stepwise mechanism for the following reaction. AKT, 2110 3. Write...
I need the mechanism please.
IV. Provide a complete stepwise mechanism for the following reaction sequence, including initiation and termination steps for any radical reactions (i.e. write a continuous reaction mechanism with the product of step 1 being used in step 2.... Draw the product of each step in the indicated boxes. 1) Br2, hv 2) KO Bu/BuOH 3) HBr, ROOR Br step 1 product step 2 product
Show all work for both please.
1.
2.
Predict the major products (A, B, C) for the following reactions. La A CH2CH2C1 AICI: B excess 1. KMnO4/NaOH/H2O 2. H30* AICI: Predict the major product for the following reaction. Explain why this is the major product and write the reaction mechanism. HNO3/H2SO4
3. Draw a stepwise, detailed mechanism for the acid-catalyzed hydration reaction in question 2 above. Use curved arrows to indicate the flow of electrons. (Note: use hydronium ion, H307, in your mechanism to indicate "acidic water"). (6 pts) 4. Draw a stepwise, detailed mechanism for the reaction below. Use curved arrows to indicate the flow of electrons. (Hint: think of this reaction as a combination of addition of HX (step 1) and hydration (step 2)]. In the second step, an...
Please show complete stepwise mechanism
Draw a stepwise mechanism for the following reaction [1] LIAIH4 CH2COCI → CH2CH2OH [2] H20
10) Write the mechanism for the following EAS reaction? 4P CL), AICI, 11) Predict the all possible products for the following reactions and circle the major product among them? 8 Pt A) -CH2 HNO3, H,SO CI, AICI, B) C) CH,CI, AICI: сна HNO.H.SO. D) OH
Write the products and the appropriate stepwise mechanism for the following reactions: (a) 1-bromobutane+ Nal (b) 2-chloro-2-methylpropane with ethanol.
Assuming it is a mono substitution reaction. Predict the products
for the following reactions and draw the mechanisms using a
stepwise arrow pushing mechanism.
HNO3 H2So4 Cassume it is a mono -substitution
Draw a stepwise mechanism for the following reaction: OH H2SO4 Part 1 out of 3 O HO HSO4 H30 finish structure ... draw structure... H2SO4
Predict the product of the following reaction and then draw a stepwise mechanism for its formation: Part 1: M OH H,804 OH H2SO4 view structure Part 2: O 0 H2O H2SO4 - > + OHSO4 view structure view structure SO2 Part 3 out of 3 0 O H2SO4 HO он H20+ 0 0 HSO4 + + - 0.0 0 window open 0 1,0 ОСН,ОН
Draw a stepwise mechanism for the following reaction: Но H2SO4 Part 1: НО" н HSO4 н OH H2SO4 view structure view structure Н,о* Part 2 out of 3 Н.о НО- H Н,о* draw structu re... window open H2SO4