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Select the keyword or phrase that will best complete each sentence. Key terms: A radical is a reactive intermediate with a si
Classify each reaction as undergoing anti-Markovnikov. Markovnikov, non-Zaitsev, or Zaitsev Br HBr ROOR non-Zaitev anti-
Determine the product(s) formed in each reaction. Br NBS hv Br Be Br HBr Be Br Br Br
Determine the reagent(s) required for the bromination of 2-methyl-1-butene. Br Br HBr PBry Br2 hv Br Br2 Br2 hv Br HBr NBS RO
Determine the reagent(s) required for the bromination of ethylcyclohexene. Br HBr NBs PBr hv HBr Br2 hv HBr ROOR NBS HBr ROOR
Determine the reagent(s) required for the bromination of cyclopentene HBr Br2 PBr3 HBr Br Br2 Br2 hv NBS hv ROORNBS hv Br2 H2
Determine the product(s) for the following reaction. Select all that apply. NB hv Br Br Br Br Br Br Br Br Br
Determine the product(s) for the following reaction. Select all that apply NBS hv Br Br Br Br Br Br Br Br. Br
1-bromobutane is synthesized from acetylene by a 4-step synthesis. Determine the appropriate reagent(s) for each step to comp
What monomer is needed to form each polymer? polymerization Cl Cl Cl polymerization Cl CI Cl a polymerization CI Cl Cl
Select the keyword or phrase that will best complete each sentence. Key terms: A radical is a reactive intermediate with a single unpaired electron, formed by homoloysis of a covalent bond. paired unpaired Allylic radicals are stabilized by resonance, making them more stable than tertiary radicals increases inductive effects A compound that contains an especially weak bond that serves as a source of radicals is called a radical initiator ess homoloysis decreases more J Treatment of cyclohexene with N-bromosuccinimide in the presence of light leads to allylic substitution by radical intermediates addition radical The stability of a radical increases as the number of alkyl groups bonded to the radical carbon increases. unselective without Although alkanes undergo radical substitution reactions with both Clh and Br2. chlorination is faster than bromination. inhibitor selective with resonance A compound that prevents radical reactions from occurring is called a radical inhibitor slower initiator Treatment of cyclohexene with bromine in an organic solvent leads to addition by ionic intermediates faster onic Radical halogenation reactions occur with racemization at a stereogenic heterolysisallylic substitution center Reset
Classify each reaction as undergoing "anti-Markovnikov". "Markovnikov, "non-Zaitsev, or "Zaitsev Br HBr ROOR non-Zaitev anti-Markovnikov HBr anti-Markovníkov Markovnikov Br Zaitev Base Zaitev Markovnikov
Determine the product(s) formed in each reaction. Br NBS hv Br Be Br HBr Be Br Br Br
Determine the reagent(s) required for the bromination of 2-methyl-1-butene. Br Br HBr PBry Br2 hv Br Br2 Br2 hv Br HBr NBS ROOR hv HBr ROOR Br FeBr но
Determine the reagent(s) required for the bromination of ethylcyclohexene. Br HBr NBs PBr hv HBr Br2 hv HBr ROOR NBS HBr ROOR Br hv NBS hv Br2 FeBry Br2 H20 Br
Determine the reagent(s) required for the bromination of cyclopentene HBr Br2 PBr3 HBr Br Br2 Br2 hv NBS hv ROORNBS hv Br2 H20 Br FeBr Br
Determine the product(s) for the following reaction. Select all that apply. NB hv Br Br Br Br Br Br Br Br Br
Determine the product(s) for the following reaction. Select all that apply NBS hv Br Br Br Br Br Br Br Br. Br
1-bromobutane is synthesized from acetylene by a 4-step synthesis. Determine the appropriate reagent(s) for each step to complete this synthesis. HBr NaH CH3CH2Br NBS, hv Br2, hv Na, NHs H2, Pd-C HBr, ROOR HBr, ROOR Na, NHs CH3CH28r NaH Br acetylene Step 4 Step 3 Step 1 Step 2
What monomer is needed to form each polymer? polymerization Cl Cl Cl polymerization Cl CI Cl a polymerization CI Cl Cl
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Answer #1

All your answers are cross-checked and found that therly are all in agreement with the chemical reaction conditions and they are all following the Markownicov's addition, Anti-Markownicov's addition rules accordingly and also Saytzef elimination in the right place. The polymerization monomers are also perfectly assigned.

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