A set of three nucleophilic displacement reactions is shown below: Br Br CH3 CH3CHCH2CH2CH2CH3 CH;CCH;CH,CH2CH3 BRCH,CHCH,CH,CH,CH3 CH3 A H20, CH;CH,OH SN1 reaction Which reaction (A, B, or C) proceeds the fastest? Which reaction (A, B, or C) proceeds the slowest?
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- A set of three nucleophilic displacement reactions is shown below: CH3 CH3 CH3 CH3 CH3 CH,CHCH,CH,CCH,CI CH,CHCH,CH,CCH,CH, CH,CHCHCH,CHCH;CH,CH, CH;CHCHCH,CH2CH,CH,CH3 CH3 CI C H2O, HCO2H 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: - 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 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: 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?Draw a detailed, step-wise mechanism for the reaction shown below. SHOW ALL BOND-FORMING AND BOND-BREAKING STEPS. SHOW ALL INTERMEDIATES. 1) NaOH 2) H3O* H3C H3C HO
- Rank the following bases in order from slowest E2 reaction rate to fastest. ONa H20 NaOH NH3 OK ONa A В D E FWhat 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 ODMinoxidil 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.
- Br 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.A set of three nucleophilic displacement reactions is shown below: CH3 A Br B CH₂CH₂Br Nal acetone SN2 reaction Which reaction (A, B, or C) proceeds the fastest? Which reaction (A, B, or C) proceeds the slowest? H3C BrDraw the mechanism for the following reaction: conc. H,SO4 Нat (c) "OH Practice Problem 07.69b1 Add curved arrow(s) to draw step 1 of the mechanism. Modify the given drawing of the product as needed to show the intermediate that is formed in this step. H CH3 CH3 CH3 -CH3 + H H. OH Edit Drawing