Give the major product(s) of the following reactions, if there is a reaction. For electrophilic aromatic substitution, assume that only one equivalent of the electrophile adds to the aromatic ring (monosubstitution). However, there may be more than one product formed. HNO3 H2SO4 OCH3 F H2SO4 NH2 1) H3C AICI3 2) H20 CI Cl2 FeCl3 `NH3

Please do by hand. Please show the mechanism for this reaction with explanation. Is it exothermic or Endothermic? Is it a SN1 reaction, SN2 reaction or Nucleophilic addition? which molecule is the electrophile and the nucleophile?

What type of substituent effect do you expect a -CC12-CC12-CC13 (perchloropropyl) group to have upon aromatic electrophilic substitution reactions? Resonance electron donor; activating substituent; ortho/para director Inductive electron donating; activating substituent; ortho/para director Resonance electron withdrawing; deactivating substituent; ortho/para director Inductive electron withdrawing; deactivating substituent; meta director

Fill in the boxes with the missing alkyl halide (reactant side), appropriate nucleophile (by arrow), or substitution or elimination product (product side). Show stereochemistry on the product when applicable. Note: "Ph" = benzene ring.

the  compound  can be synthesized by an SN2 reaction. Suggest a combination of haloalkane and nucleophile that will give each product.

Give detailed Solution with explanation needed. don't use Ai for answering this

electrophilic aromatic substitution reactions. type op or m, to indicate if the group would be an op or meta director in b H H H H h H CH3 blank 1 blank 2 blank 3 blank 4 blank 5 blank 6 :O: HLYXHOX CH3 CH₂CH3 blank 7 -CH3 C=N: blank 8 blank 9 blank 10 blank 11

Please don't provide handwritten solution......

In electrophilic aromatic substitution, a group attached to the aromatic ring does not affect ring reactivity. Is that true or false?

The conversion of alcohols into alkyl halides by reaction with hydrogen halides is an example of a Nucleophilic Substitution Reaction. This kind of reaction can proceed by two different mechanisms depending on the structure of alcohol substrates used. Generally, primary alcohols are substituted via SN2 mechanism, while secondary and tertiary alcohols undergo SN1 mechanism. Consider the following reaction given in the picture below and the questions in the picture too.