The given reaction scheme is an example of which type of reaction? O || R₁-C-OH + R₂-OH Oxidation Fischer esterification Nucleophilic substitution Acid O || R₂₁-C-O-R₂
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- + F₂ catalyst The above reactants would undergo a catalyst .ل= + H H The above reaction would be an example of HHHH |||| H-C=C-C-C-C-C-H+2H-H | | | | HHHH The above reactants would undergo a(n) catalyst reaction ◆ reaction Isopropyl alcohol (propan-2-ol) is used as a solvent for industrial processes, a disinfectant solution, and a de-icer solution for vehicles. One method of producing isopropyl alcohol is to react propene with water in the presence of an acid catalyst. This reaction is classified as a(n) ◆ reaction.What is the predicted product of the reaction sequence shown? OH excess NH3 NazCr2O7/H2SO4/H2O SOCI2 SOCI2 1. CH3CH₂MgBr 2. HO H || میں بلی HO. NH2 |||1c. What is the nucleophile in the following reaction? .Br CH;CO0 Na LO OCCH3 NaBr ld. What is the electrophile in the following reaction? Br CH;COO Na L0OCCH3 NaBr +
- esc ||| = O PRINCIPLES OF ORGANIC CHEMISTRY Classifying organic reactions Classify each of the following as either a substitution, elimination, or addition reaction. Explanation < xe Br y Check K* "OC(CH3)3 Fe catalyst Q A + Br₂- + H₂0 H hv -xx +H₂- Pd/C + H₂ Br OH + HBr + HBr e O substitution O elimination O addition. substitution elimination addition substitution elimination addition substitution O elimination O addition O substitution O elimination. addition MacBook Pro X Ś 4/5 Kimberly V ? S ⠀⠀ ol Ar D © 2023 McGraw Hill LLC. All Rights Reserved. Terms of Use | Privacy Center | AccessibiliComplete the reactions given below H+/isi OH c)1. y which mainly › time, net- ral rent ters. Phenobarbital 1090 10 Following is a structural formula for aspartame, an ar- tificial sweetener about 180 times as sweet as sucrose (table sugar). O NH3 H egy N Aspartame HOO HO HO HOOH + HO O OCH3 (f) Draw structural formulas for the products of com- plete hydrolysis of aspartame in aqueous NaOH. Show each product as it would be ionized in this solution.
- The order from most reactive to least reactive with aqueous ammonia is (А) CH--o-č-CH, * CH,--oCH,CH, * CH,--a CH--č-OCH,CH, ° CH,--c³ CH---o-č-CH, > CH3-C-OCH2CH3 | CH3-C-CI | (В) %3D > CH3-C-CI CH3-C-0-C-CH3 (C) > CH3-C-CI CH3-C-OCH2CH3 CH3-C-0-C-CH3 (D) || > CH3-C-CI CH3-C-0-C-CH3 CH3-C-OCH2CH3OPh OPh D CI Br N E N Но o-SiMeg OH OPh OPh F NH2 Но N Но OH OH A V ( Choose ] Bu4N+ F- МСРВА (Ваyer villager) Mg, then CO2 (Kobe!!!!) NH3 (SNAR) H2S04, Heat (Fisher esterification) 03, DMS (ozonalysis) Choose (Choose ) E [ Choose ) F [ Choose ) B.Reaction C Select Draw Rings More |||||| C 0 N H 0 || H H₂C C-C I heat H₂C CH–COOH +CH,CH(CH,)NH, H₂C- CH₂ H₂C J Q2Q Draw the amide formed when isopropylamine (CH₂CH(CH³)NH₂) (CH3CH(CH3)NH₂) is heated with each carboxylic acid. Include all hydrogen atoms. What did I do wrong? N HC- Erase CH₂
- MAIN QUESTION Acyl transfer: ester saponification Question 1 of 5 Write the first step of the reaction mechanism using curved arrows to show electron reorganization. Electron pairs ERASE H₂C-C CH3 OCH3 - NaOH H₂O -H₂C-00 :O: || C | :O-CH3 O Na H-O-CH3 I H :O: H-O- -H I Na + SubmitWhich statement is false regarding the following system? + HX Addition Elimination H -X O A positive AG means that the equilibrium will favor the reactants because the entropy term is larger than the enthalpy term representing the gain of entropy when one molecule becomes two. O A negative AG means that the equilibrium will favor the products because the enthalpy term is larger than the entropy term representing the loss of entropy when two molecules become one. Elimination reactions are thermodynamically favored at high temperatures, where the entropy of the reaction will be larger than the enthalpy, causing a positive AG and the reactants to be favored over the products. Addition reactions are thermodynamically favored at high temperatures, where the entropy of the reaction will be larger than the enthalpy, causing a positive AG and the reactants to be favored over the products.Rank the following carboxylic acid derivatives in decreasing order (most to least) of reactivity towards nucleophilic substitution. O I > IV > II| > || O || > ||| > IV > I O | > ||| > | > IV O III > IV> | > | O IV > I > III > || = ||| CI OCH3 11 IV NH₂ ONa