or Me OMe

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from compound 3 to 4, the nitro group in compound 3 is going through [ hydrolysis / reduction / substitution / oxidation] to afford compound 4

1) Complete the following reaction and provide a detailed, step-by-step mechanism for the process. HBr 2) Provide the structure of the major organic product in the reactions below. HI CH3 win H3C. CH3 CH₂CH3 HCI Xero H₂C CH3 HBr

Please explain step by

The synthesis shown above can be accomplished in three steps. Select the reagents for each step from the dropdown lists below.

Hello, If you could please help me solve this problem. These are the options for each reagent.  1:  HCl/H2OHCl/H2O CH3NH2CH3⁢NH2 NaOH/H2ONaOH/H2O methanol 2:  NaOH/H2O CH3NH2 methanol HCl/H2O 5. NaOH/H2O CH3NH2 methanol HCl/H2O 6 NaOH/H2O CH3NH2 methanol HCl/H2O

Rank the alkyl halides in order of increasing E2 reactivity. Then do the same for E1 reactivity. CI Br A C

Please help with explanation need.

E. Show the products in the following reactions. If more than one product is possible, label the major product. H3CO O NO₂ SO3, H₂SO4 SO3H NO₂ Br₂, FeBr3 CH3I, AIC13 HNO3, H₂SO4