Product A Product B Product C a. The reagents that would selectively yield Product A are [ Select] b. The reagents that would selectively yield Product B are [ Select] C. The reagents that would selectively yield Product C are [ Select]
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![Use the image below to answer the following three questions. Note: Subscripts are
not shown in answer choices, ex: H2 should be H2, NH3 should be NH3.
Product A
Product B
Product C
a. The reagents that would selectively yield ProductA are
[ Select]
b. The reagents that would selectively yield Product B are
[Select]
c. The reagents that would selectively yield Product Care
[Select]](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2Fd1272796-fc0f-416a-81a3-03a4c523ec88%2Fbb497c34-559d-4b1e-b6bc-12b9d3619ec5%2Fee92ux_processed.jpeg&w=3840&q=75)
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- 4. Circle the electrophilic and nucleophilic atoms in each substitution reaction below. Provide the neutral organic product; where a stereocenter is created, use a wavy bond to indicate a mixture of configurations or wedges/dashes for stereospecific reactions. Also, provide the dominant reaction mechanism (Sn2 or SN1) somewhere in each box. A. Br NaSEt DMF В. ELOH C. .SO2NHNA Cl + D. NaH Br- HO, DMFWhich reaction (s) does an anhydride produce? HO. NEl3 CI КОН I. calor OK II NH2 O. IV HO HO. calor III a. Ob., IV Oc. I, II d., II, III, IVUse the image below to answer the following three questions. Note: Subscripts are not shown in answer choices, ex: H2 should be H2, NH3 should be NH3. Product A Product B Product C a. The reagents that would selectively yield Product A are [Select] b. The reagents that would selectively yield Product B are [ Sclect] c. The reagents that would selectively yield Product C are [ Select]
- ited Draw both resonance structures of the most stable carbocation intermediate in the reaction shown. od m... • You do not have to consider stereochemistry. . Do not include anionic counter-ions, e.g., I', in your answer. • Draw one structure per sketcher. Add additional sketchers using the drop-down menu in the bottom Separate resonance structures using the → symbol from the drop-down menu. ● CH4 + ? HBr3. Draw all products for the following reactions. For your products, write whether the nucleophile added to the Re face or Si face of the starting material. a. HO b. 1) LIAIH 2) H™ 1) CH3CH2Li 2) H+ c) Determine whether the nucleophile added to the Re face or Si face of benzaldehyde.Question 4 4. Draw the final major product(s) for each multistep synthesis reaction. H3O* OMe H3PO4 Jones EtzNH reagent H30* 1. O3 NABH3CN PBr3 KOC(CH3)3 -OH 2. DMS NH3, H3O* Br KOC(CH3)3 1. ВНз РСС H30* 2. HаОг, ОН CH2CI2
- 4. Draw the product to each of the following reactions. a. b. C. d. CHO HO H HO- H 1) NH₂OH H OH 2) Ac₂O, heat HO- -H 3) NaOH, H₂O CH₂OH CHO HO -H HO H HO H CH₂OH CHO 1) HCI, NaCN 2) H2, Lindlar's catalyst 3) HCI, H₂O HO 1) NH₂OH -H 2) Ac₂O, heat HO- -H 3) NaOH, H₂O H -OH CH₂OH CHO 1) HCI, NaCN H -OH 2) H2, Lindlar's catalyst HO- -H 3) HCI, H₂O CH₂OHUse the dropdown menu to indicate whether the rate of the reaction shown below will increase, decrease, or remain the same when the reaction conditions are changed to X or to Y or to Z (see below). NaN3 'N3 Br CH3CN X: Change the leaving group from Br to CI Y: Increase the concentration of haloalkane Z: Increase the concentration of NaN3 X: choose your answer.. ^ Y: choose your answer... V Z: choose your answer... choose your answer... Remain the same Nex Decrease Increase2. Но ... H-O Draw the major product of this reaction. Explain your reasoning. Br₂, H₂O EtOH 1. Me₂ BuSi-CI, imidazole 2.9-BBN-H (like BH3) 3. H₂O₂, NaOH OTMS excess HBr
- Draw the major product of this reaction. Ignore inorganic byproducts. 1. CrO3, H2SO4 H 2. Neutralizing work-up DrawingDraw the major product of this reaction. Ignore inorganic byproducts. 0 1. CrO3, H₂SO4 2. Neutralizing work-up H .What is the product of this reaction sequence? B. ОН A OB OC OD НО 2. LiAIH4 3. H2O, H, heat ОН _OH H+ D. ОН ? ОН