A set of three nucleophilic displacement reactions is shown below: CH3 CH3 CH3 CH3 CH3 CH3CHCH,CH,ČCH2CI CH3CHCH,CH,CCHCH3 CH;CHCHCH,CHCH2CH,CH3 ČH3 A H20, HCO2H SN1 reaction Which reaction (A, B, or C) proceeds the fastest? Which reaction (A, B, or C) proceeds the slowest? B.
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- A set of three nucleophilic displacement reactions is shown below: Br CH3 BRCH,CHCH,CH,CH,CH3 Br CH3CHCH,CH,CH,CH3 CH3CCH,CH2CH,CH3 CH3 A B H20, CH;CH,OH SN1 reaction Which reaction (A, B, or C) proceeds the fastest? Which reaction (A, B, or C) proceeds the slowest?A set of three nucleophilic displacement reactions is shown below: CH3 CH3 CH3 CH3 CH3 CH3CHCH2CH2ČCH2CI CH3CHCH2CH2ĊCH2CH3 CH;CHCHCH,CH2CH,CH,CH3 ČH3 ĆI C CI A H2O, HCO2H SN1 reaction Which reaction (A, B, or C) proceeds the fastest? Which reaction (A, B, or C) proceeds the slowest? Submit Answer Retry Entire Group 9 more group attempts remainingA set of three nucleophilic displacement reactions is shown below: - Br -Br -Br "CHз Hзс CHз C В A NaCN CH-он SN2 reaction Which reaction (A, B, or C) proceeds the fastest? Which reaction (A, B, or C) proceeds the slowest?
- A set of three nucleophilic displacement reactions is shown below: CH3 SOH CH;CH,CCH3 SN1 reaction Br A, SOH = 100% CH3OH B, SOH = 33% CH3OH, 67% H2O C, SOH = 67% CH3OH, 33% H2O Which reaction (A, B, or C) proceeds the fastest? Which reaction (A, B, or C) proceeds the slowest?A set of three nucleophilic displacement reactions is shown below: CH3 SOH CH3CH2CCH3 SN1 reaction Br А, SOH %3D 100% CH,ОН В, SOH 3 33% Cн,он, 67% H20 С, SOH %3D 67% CH3ОН, 33% H20 Which reaction (A, B, or C) proceeds the fastest? Which reaction (A, B, or C) proceeds the slowest?What is the outcome of the series of reactions shown in the box? OH OCH3 HNO3 Sn or Fe NaNO2 H3CO H2SO4 HCI H2SO4, H2O OCH3 H3CO NO2 A) B) OH HO LOCH3 C) LOCH3 D) H3CO H3CO y-N OH A В OD
- What is the expected major product of this reaction? OH H₂N I H₂N H₂N 85% H3PO4, A H₂N ||| ? H₂N IVBr CH3OH + Br-Br H3CO The mechanism proceeds through a first cationic intermediate, intermediate 1. Nucleophilic attack leads to intermediate 2, which goes on to form the final product. In cases that involve a negatively charged nucleophile, the attack of the nucleophile leads directly to the product. +Br + CH3OH Br Intermediate 1 Intermediate 2 (product) In a similar fashion, draw intermediate 1 and intermediate 2 (final product) for the following reaction. OH + Br2 + HBr Br racemic mixture • Pay attention to the reactants, they may differ from the examples. In some reactions, one part of the molecule acts as the nucleophile. • You do not have to consider stereochemistry. • Draw one structure per sketcher. Add additional sketchers using the drop-down menu in the bottom right corner. Separate intermediate 1 and intermediate 2 using the → symbol from the dropdown menu.Predict the product of each reaction or sequence of reactions. a) b) Na₂Cr₂O7 H₂SO4, H₂O 1. NBS, A 2. t-BUOK 1. NBS, A 2. NACECH e) 1. NBS, A 2. t-BuOK 3. HCI 1. NBS, A 2. Mg O 3.
- Identify compounds A-I in the following synthesis scheme. CUCN D conc HNO3 1. HCI, Fe NaNO2 A 2. NaOH В HCI Same as above Br2 Mg(s). F Et,0 1. D NaBH4 1. NaH >E FeBr3 G ELOH 2. H2О (еxcess), H,SO4 2. C6H5CH,BrChoose the best reagents to complete the reaction shown below. 1118 1. PhMgBr 2. H3O+ OH "Br a (P) A B C D E conc. HBr 1. LiAlH4 2. H3O* 1. H3O+ 2. NaBH4 1. PhLi 2. H3O+ 1. PhMgBr 2. H3O+Minoxidil is a molecule that causes hair growth in some people. It was originally synthesized as a vasodilator for the treatment of hypertension (high blood pressure). Most of the patients taking the drug for hypertension were seen to grow body hair. Due to other side effects, its oral use was stopped, but it became popular as a topical cream to promote hair growth. NH2 N-OH NH Minoxidil The first key reaction in one synthesis of minoxidil follows. Draw the product of this reaction. NH NC.