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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What is Wrong? Select the keyword or phrase that will best complete each sentence. Key terms: A radical...
In each reaction box, place the best reagent and conditions from the list below. 1) 2) Br 3) CH3CH2CH2CI, AlCl3 HNO3. H2S04 NBS, ROOR, hv H2 CH3CH2Cl, AICla , AICI AlCl3 NaBH4 Br2, FeBr3 Cl Zn(Hg), HCI Br2 In each reaction box, place the best reagent and conditions from the list below. 1) CHyCH2CH2CI, AlCl 2) 3) 4) mCPBA Pd, H2 BH3THF (CH3)3CO Br2, H20 CHCOO S ROR Br2, FeBr3 HBr Br2 In each reaction box, place the best reagent...
Select the keyword or phrase that will best complete each sentence. Key terms: Alkyl halides undergo substitution reactions with nucleophiles. Strong nucleophiles favor the mechanism. mechanism over the carbocation An SN1 mechanism forms a carbocation as a reactive intermediate and the mechanism has two steps. elimination nucleophile Protic solvents favor mechanism and aprotic solvents favor the one step reactions proceed with racemization at a single stereogenic center substitution three steps Increasing alkyl substitution favors an decreasing alkyl substitution favors an...
1. please check what is wrong. Thank you! Determine the product formed when each compound is treated with Br2 and FeBr3. Drag the atom labels to their appropriate positions. CN Atom labels H H Br Br2 A. FeBr Br H OH OH Br Br. Br2 FeBr3 H H Br Br H Br2 FeBr H1 H Reset T Rank the compounds in each group in order of decreasing reactivity in electrophilic aromatic substitution. CI Decreasing reactivity Rank the compounds in each...
Propose an efficient synthesis for the transformation below, using two sequential reductive aminations. Enter the appropriate number or letter from the reagent list handout. Propose an efficient synthesis for the transformation below, using two sequential reductive aminations. Enter the appropriate number or letter from the reagent list handout. Step 1 + NaBH3CN, H+, Step 2 - NaBH3CN, H+ Reagent List (Updated 4/30/2020) Enter # or letter in the appropriate boxes. Note: Exam responses are case insensitive Alkyl Halides (X = Cl,...