SavedDetermine if the organic substrate is oxidized or reduced in the following reaction. Select the single bestanswer.+ 2NaNH,CH3CH CH,CH3C CH + 2Na + 2NH3CThe organic substrate is reduced.The organic substrate is oxidized.Next>1 of 13Wto searchupinsnnf12hof8144f6fs4

Hydrogenation of an Alkyne to an Alkene (trans-alkene):Alkynes can be reduced to trans-alkenes with…

Answered: Saved Determine if the organic…

Organic Chemistry

8th Edition

ISBN:9781305580350

Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote

Publisher:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote

Chapter18: Functional Derivatives Of Carboxylic Acids

Section: Chapter Questions

Problem 18.69P

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Complete and balance the following methesis reaction in aqueous solution.Answer Entery Instructions• Parentheses are only required around polyatomic ions and only when more than 1 of those ions is present.K3PO4 (no parentheses required).Mg3(PO4)2 (parentheses required).• In each case one product is soluble (aq) and one insoluble (s). Use solubility rules to determine which product appears in each box.***Answer*** Na2S (aq) + ***Answer*** FeCl3 (aq) ➝ ***Answer*** ***Answer*** (s) + ***Answer *** ***Answer*** (aq)
21-25 Draw the major organic product of the reactions
What is the product (from the image below) of the starting material D-glyceraldehyde which will (1) produce aldaric acid upon reacting with HNO3 + H2O, NaOCH2, NH2OH, and (CH3CO)2O + NaOCOCH3 (2) produce tartaric acid upon reacting with HNO3 + H2O, NaOCH3, NH2OH, and (CH3CO)2O + NaOCOCH3
What is the product of the starting material D-glyceraldehyde which will (1) produce aldaric acid upon reacting with HNO3 + H2O, NaOCH2, NH2OH, and (CH3CO)2O + NaOCOCH3 (2) produce tartaric acid upon reacting with HNO3 + H2O, NaOCH3, NH2OH, and (CH3CO)2O + NaOCOCH3
Identify the organic functional groups and reaction type for the following reaction.Please include everything including the letter and the answers.The reactant is a(n)a. amideb. aldehydec. alcohold. carboxylic acide. esterf. ketoneThe product is a(n)a. carboxlyate ionb. ammonium ionc. alcohold. carboxylic acide. ketonef. aldehydeThe reaction type isa. hydrationb. esterificationc. hydrolysis (in acid)d. hydrolysis (in base)e. amide synthesisf. amide synthesisg. dehydrationh. acid base
pls match them with the options, thats all What is the purpose of using the following chemicals in the preparation of n-butyl acetate? 1. Na2CO3 2. H2SO4 3. MgSO4 4. CH3COOH options: It is used as a dehydrating agent It is used as a catalyst It is used as a neutralizing substance for excess acid It is one of the reactant
Draw the product of the reactions of succinic anhydride with each of the listed reagents. Assume in all cases that the reagent is present in excess and an aqueous workup takes place after each reaction. A. Reaction with (CH3)2CHOH. \table[[Select,Draw,Templates More,,],[/,//,I//,H,Erase]] B. Reaction with NH3. \table[[Select,Draw,tes More,Erase],[/,//,III,C,H,N,0]] Question Source: Vollhardt 7e0 Organic Chemistry: Structure And Function Publishęr: W. Freemar C. Reaction with phenylmagnesium bromide in THF, followed by H+,H2o. \table[[Select,Drav,v T,lates,,,Erase],[1,II,III,C,H,0,]] D. Reaction with LiAlH4 in ether, followed by H+,H2O \table[[Select,Draw,Templates More],[/,//,III]] \table[[3,0]] \table[[,2,Q
Draw the structure of the organic product expected when BrCH2CH(CH3)CH2OH is treated with base.
What product is formed when attached compound is treated with either Ag2O, NH4OH or Na2Cr2O7, H2SO4, H2O?
Which of the following method is the best method for the synthesis of propanoic acid A.) Method: Fischer esterification, Reactant: HCl, Substrates: Methanol & ethanoic acid B.) Method: Haloform reaction, Reactants: Br₂ & NaOH, Substrate: Propanone C.) Method: Oxidation, Reactant: KMnO₄, Substrate: 3-hexene D.) Method: Hydrolysis of Cyanohydrins, Reactant: HCN & HCl, Substrate: Propanone E.) None of the given choices
Which of the following method is the best method for the synthesis of hexanal A.) Method: Ozonolysis, Reactant: Ozone, Substrate: 1-cyclopentyl-1-hexene B.) Method: Reduction, Reactant: LiAlH₄, Substrate: hexanoic acid C.) Method: Oxidation, Reactant: H₂CrO₄, Substrate: hexanol D.) Method: Oxidation, Reactant: KMnO₄, Substrate: hexanol E.) None of the given choices
Which of the following reducing agents will result to the formation of 3-hydroxypentanoic acid when reacted with 3-oxopentanoic acid? -- LiAlH4 -- NaBH4 -- H2/Pt -- H2/Linlar’s catalyst

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Saved Determine if the organic substrate is oxidized or reduced in the following reaction. Select the single best answer. + 2NaNH, CH3CH CH, CH3C CH + 2Na + 2NH3C The organic substrate is reduced. The organic substrate is oxidized. Next> 1 of 13 W to search up ins nn f12 ho f8 144 f6 fs 4