Draw the major product of the aldol condensation reaction between two of equivalents of this aldehyde with the conditions provided. Ignore inorganic byproducts. 1. H3O+, heat H 2. Neutralizing work-up
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- My Home OWLV2 | Online teaching and lear X G D /ilrn/takeAssignment/takeCovalentActivity.do?locator=assignment-take IReviaw Toples Draw structures for the carbonyl electrophile and enolate nucleophile that react to give the enone below. You do not have to consider stereochemistry. Draw the enolate ion in its carbanion form. Draw one structure per sketcher. Add additional sketchers using the drop-down menu in the bottom right comer. Separate multiple reactants using the + sign from the drop-down menu. aste [F ChemDoode Submit Anewer Retry Entro Group 8 more group attempts remainingProvide a stepwise synthesis of 1-cyclopentylethanamine using the Gabriel synthesis. NH NK NH HO. OH NH2 Кон; ;H3O+ KOH; ;H30* "Br LIAIH4; ; H3O* Br LIAIH4;(d) Explain the observed stereo-selectivity in the formation of product using Chelation model. OMe H3CQ Ph. Ph- Zn(BH4)2, CH2CH3 `CH2CH3 H OH THE
- Why do you suppose ketone halogenations in acidic media are referred to as being acid-catalyzed, whereas halogenations in basic media are base-promoted? In other words, why is a full equivalent of base required for halogenation?raw the major product of this reaction. Ignore inor byproducts. sume that the water side product is continuously re to drive the reaction toward products. O CH3CH2NH2, TSOH Drawing OQUESTION 18 Consider the ether cleavage reaction shown below. What mechanism occurs and what are the major organic products of the reaction? 1 eq. HCI ponding letter designation O A. Mechanism: S2, Products: B.. Mechanism: SN1, Products: OC. Mechanism: SN1, Products: CI HO D.. Mechanism: SN2, Products: HO
- Synthesis - Drawing Saved Synthesize the following compound from cyclohexanol, ethanol, and any other needed reagents. он Part 1 out of 2 plnts Preparation of organometallic reagent: еВook Print References A B CH3CH2OH CH3 CH2MGB. draw structure ... Draw the intermediate product above and select the correct reagent for A. O Br, O NaBr O HBr O Select the correct reagent for B. O Mg O MgBr2 O MgI, O MgO Hin Soluti raw 11 e here to searchWhat is the cruved arrow mechanism for the reaction of p-bromo benzaldehyde treated with bromine/FeBr3. Include all resonance forms for the formation of the major product as well as the number of different carbons on the final product. Thank you for the help!e. Name the major product/s of this reaction only. 1,2,2-trimethylcyclopentan-1-ol is heated in aqueous sulfuric acid f. (3S, 4S)-4-methyl-3-hexanol is heated in aqueous sulfuric acid
- The chromake and maganle esters shown below form the reachon of 3-butene-2-ol unth on romic aud and maganese dioxide (Mn0z) respectively. They both de ompose to give metny lunul ketone throuah me chanish cally dishing pathway s. 1.Kive mechanism for manganale ester decomposıhon. 2 Indıcale wnich intermediate in the meenanirm rahronalizes the observahon that only allylic and benrylie dalcohols heact mth Mn0z to give (arbonul products. %3D :cr-oH chromale ester methyl unyl kehone (A) :mn COH), manganale ester methyl uiny| kehoneK Curved arrows are used to illustrate the flow of electrons. Follow the curved arrows and draw the structure of the missing reactants, intermediates, or products in the following mechanism. Include all lone pairs. Ignore stereochemistry. Ignore inorganic byproducts. H. H. THE BH₂ BH₂ Draw Major Borane Intermediate Problem1.Draw the structures of all 3 resonance hybrid forms of the benzenonium intermediatefor both o and p attack for the case of activating groups an indicate which one in eachcase is the most stable form.Draw the structure of all 3 resonance hybrid forms of the benzenonium intermediatefor m attack in the case involving a deactivating group. 2.Halogens are deactivating groups but direct electrophilic attack at the o and ppositions. Why is this the case?