a. Label the reactive features of the following reactants, select the most reactive feature, then write and highlight what it needs. Also, state if a carbocation, carbon radical, or carbanion will start to develop, and/or if aromatic character will be lost as a result of a reaction between these molecules. benzenesulfonic acid + Cl; and FeCl, b. Use mechanism arrows to illustrate the reaction that occurs.
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- Label the reactive features of the following reactants, select the most reactive feature, thenwrite and highlight what it needs. Also, state if a carbocation, carbon radical, or carbanion willstart to develop, and/or if aromatic character will be lost as a result of a reaction between thesemolecules.(E)-4,5-dimethyloct-4-ene + HBr and H2O2(a) For which aromatic compound do you expect nitration to take place faster: furan or thiophene? (b) For each of these compounds, at which C atom do you expectelectrophilic aromatic substitution to predominantly takeplace? Explain your reasoning.Label the reactive features of the following reactants, select the most reactive feature, thenwrite and highlight what it needs. Also, state if a carbocation, carbon radical, or carbanion willstart to develop, and/or if aromatic character will be lost as a result of a reaction between thesemolecules.1,2-dimethylcyclopentene + Br2 in water
- Consider the reaction: Draw out the two possible substitution reaction pathways (SN1 and SN2) and include all possible products. Include the structure of any intermediates and provide the curly arrow mechanisms required for both pathways. Using your answer to the above, justify which reaction pathway (SN1 or SN2) is more likely to occurLabel the reactive features of the following reactants, select the most reactive feature, thenwrite and highlight what it needs. Also, state if a carbocation, carbon radical, or carbanion willstart to develop, and/or if aromatic character will be lost as a result of a reaction between thesemolecules. 2-methylcyclohexa-1,3-diene with Cl2Provide a reaction that shows Free radical substitution.
- PLEASE, I DO NOT UNDERSTAND IT, AND NOTHING IS HELPING. STEPS LEADING TO THE CORRECT ANSWER WOULD BE HELPFUL! BOND LINE DRAWINGS PLEASE. Question: Draw the missing products or reagants in the following multistep synthesis. Ignore any inorganic byproducts.Label the reactive features of the following reactants, select the most reactive feature, thenwrite and highlight what it needs. Also, state if a carbocation, carbon radical, or carbanion willstart to develop, and/or if aromatic character will be lost as a result of a reaction between thesemolecules.2 equivalents of ethyl ethanoate + potassium ethoxide in ethanolIf there are unshared pairs of electrons on the atoms directly attached to the aromatic ring, they are the groups that provide electrons to the ring with the effect of ……………… and are ………………… directive towards electrophiles. Groups that are double bonded to a more electronegative atom than the atoms directly attached to the ring are ……… steers that withdraw electrons from the ring with the effect of .................. Groups whose electronegativity is higher than the sp2 carbon of the ring directly attached to the ring will withdraw electrons from the ring as ............. and ……… they are routers. Halogens, on the other hand, withdraw electrons from the ring as ………......... due to their high electronegativity and are ……….. directing. A. Resonance/(o-, p-)/ resonance/(m-)/ inductive/(o-, p-)/ inductive/(o-, p-) B. Resonance/(o-, p-)/ resonance/(m-)/ inductive/(o-, p-)/ inductive/(m-) C. Resonance/(o-, p-)/ resonance/(m-)/ inductive/(m-)/ inductive/(o-, p-) D. Inductive/(o-, p-)/…
- Label the reactive features of the following reactants, select the most reactive feature, thenwrite and highlight what it needs. Also, state if a carbocation, carbon radical, or carbanion willstart to develop, and/or if aromatic character will be lost as a result of a reaction between thesemolecules. cyclohexanone + 2 equivalents of methanol with acidExplain very detailed why the nitro group add to the ortho of the methyl and not to the Tbutyl group. Please use electron donating and withdrawing groups in the explanation as well as electron density.Kindly Draw the Full mechanism (with electron pushing and formal charges) for the Wolff-kishner reduction of Isatin. DO NOT skip any steps please. From beginning to end - include proper electron / arrow pushing. And at the end, in a sentence, write what the side products of the reduction of isatin are. [I asked this question before aswell but it wasn't answered up to par, so kindly do exactly what needs to be done, please and thank you]