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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
molecules.
bromobenzene + 2-chloro-3-methyl butane + AlCl3
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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.1,2-dimethylcyclopentene + Br2 in waterLabel 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 acidLabel 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 ethanol
- 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-methylcyclohexa-1,3-diene with Cl2Discuss the regioselectivity of the compound equation below, including in your answer the terms: radical plusstable, homolytic breakage, main product.If you want to disrupt the ability of radicals to generate more of themselves, particularly in scenarios where they could be harmful like auto-oxidation, you need to find a suitable scavenger reagent. Such materials, known as antioxidants, succeed when they can lead to a new, more stable radical species that terminates the chain without reacting, or by further consumption of reactive radicals to generate additional non-radical species. Which species(s) is or are radical-scavenging reagent(s)? * I just II, only III, only IV, only I and II, only II and III, only III and IV, only
- For each of the following, write the major product(s) and then draw out each step in the mechanism using curved arrows. Show ALL lone pair electrons and formal charges. Redraw ALL molecules as to show explicitly ALL bonds being broken or formed. Identify the molecular orbital (HOMO) of the nucleophile and the molecular orbital (LUMO) of electrophile involved in the nucleophilic attack. MO diagrams are not necessary..1-bromo-2-methylpropane can be synthesized from tert-butanol in two steps. Provide a synthesis route that uses a radical-based process.By using FMO principles, complete and predict the regioselectivity of the following pericyclic reaction:
- Provide a reaction that shows Free radical substitution.Please provide bond energy dissociation accurately for these 3 bonds for the below structure (with reference must be from a book or an article which I can find please): between carbon - carbon within the aromatic ring; between carbon - carbon between two aromatic rings; and between carbon - hydrogen within the aromatic ring. Thanks so much for your help!fill in the blanks. If 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.
