(a)
Interpretation:
The structural formula of reaction products in saponification using sodium hydroxide for the given ester has to be written.
Concept Introduction:
Breaking of the carbon‑oxygen single bond present between the “acid part” and “alcohol part” is one of the important reactions of ester. This process of breaking the bond between the carbon‑oxygen is known as ester hydrolysis or saponification. The condition prevails in the reaction determines it as ester hydrolysis of saponification.
Ester hydrolysis takes place in ester when it is treated with strong acid or enzymes as catalyst. Reverse of esterification reaction is the ester hydrolysis.
Saponification is the reaction that ester undergoes when a strong base is used to give the product as
(b)
Interpretation:
The structural formula of reaction products in saponification using sodium hydroxide for the given ester has to be written.
Concept Introduction:
Breaking of the carbon‑oxygen single bond present between the “acid part” and “alcohol part” is one of the important reactions of ester. This process of breaking the bond between the carbon‑oxygen is known as ester hydrolysis or saponification. The condition prevails in the reaction determines it as ester hydrolysis of saponification.
Ester hydrolysis takes place in ester when it is treated with strong acid or enzymes as catalyst. Reverse of esterification reaction is the ester hydrolysis.
Saponification is the reaction that ester undergoes when a strong base is used to give the product as carboxylic acid salt and alcohol.
(c)
Interpretation:
The structural formula of reaction products in saponification using sodium hydroxide for the given ester has to be written.
Concept Introduction:
Breaking of the carbon‑oxygen single bond present between the “acid part” and “alcohol part” is one of the important reactions of ester. This process of breaking the bond between the carbon‑oxygen is known as ester hydrolysis or saponification. The condition prevails in the reaction determines it as ester hydrolysis of saponification.
Ester hydrolysis takes place in ester when it is treated with strong acid or enzymes as catalyst. Reverse of esterification reaction is the ester hydrolysis.
Saponification is the reaction that ester undergoes when a strong base is used to give the product as carboxylic acid salt and alcohol.
(d)
Interpretation:
The structural formula of reaction products in saponification using sodium hydroxide for the given ester has to be written.
Concept Introduction:
Breaking of the carbon‑oxygen single bond present between the “acid part” and “alcohol part” is one of the important reactions of ester. This process of breaking the bond between the carbon‑oxygen is known as ester hydrolysis or saponification. The condition prevails in the reaction determines it as ester hydrolysis of saponification.
Ester hydrolysis takes place in ester when it is treated with strong acid or enzymes as catalyst. Reverse of esterification reaction is the ester hydrolysis.
Saponification is the reaction that ester undergoes when a strong base is used to give the product as carboxylic acid salt and alcohol.
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Chapter 16 Solutions
EBK GENERAL, ORGANIC, AND BIOLOGICAL CH
- Safari File Edit View History Bookmarks Window Help く < mylabmastering.pearson.com Wed Feb 12 8:44 PM ✩ + Apple Q Bing Google SignOutOptions M Question 36 - Lab HW BI... P Pearson MyLab and Mast... P Course Home Error | bartleby b Answered: If the biosynth... Draw a free-radical mechanism for the following reaction, forming the major monobromination product: ScreenPal - 2022 CHEM2... Access Pearson 2 CH3 Br-Br CH H3 Draw all missing reactants and/or products in the appropriate boxes by placing atoms on the canvas and connecting them with bonds. Add charges where needed. Electron- flow arrows should start on the electron(s) of an atom or a bond and should end on an atom, bond, or location where a new bond should be created. Include all free radicals by right-clicking on an atom on the canvas and then using the Atom properties to select the monovalent radical. ▸ View Available Hint(s) 0 2 DE [1] H EXP. CONT. H. Br-Br H FEB 12arrow_forwardPlease correct answer and don't use hand ratingarrow_forwardNonearrow_forwardQ1: For each molecule, assign each stereocenter as R or S. Circle the meso compounds. Label each compound as chiral or achiral. + CI Br : Н OH H wo་ཡིག་ཐrow HO 3 D ။။ဂ CI Br H, CI Br Br H₂N OMe R IN I I N S H Br ជ័យ CI CI D OHarrow_forwardPlease correct answer and don't use hand ratingarrow_forwardNonearrow_forward%Reflectance 95 90- 85 22 00 89 60 55 50 70 65 75 80 50- 45 40 WA 35 30- 25 20- 4000 3500 Date: Thu Feb 06 17:21:21 2025 (GMT-05:0(UnknownD Scans: 8 Resolution: 2.000 3000 2500 Wavenumbers (cm-1) 100- 2981.77 1734.25 2000 1500 1000 1372.09 1108.01 2359.09 1469.82 1181.94 1145.20 1017.01 958.45 886.97 820.49 668.25 630.05 611.37arrow_forwardNonearrow_forwardCH3 CH H3C CH3 H OH H3C- -OCH2CH3 H3C H -OCH3 For each of the above compounds, do the following: 1. List the wave numbers of all the IR bands in the 1350-4000 cm-1 region. For each one, state what bond or group it represents. 2. Label equivalent sets of protons with lower-case letters. Then, for each 1H NMR signal, give the 8 value, the type of splitting (singlet, doublet etc.), and the number protons it represents. of letter δ value splitting # of protons 3. Redraw the compound and label equivalent sets of carbons with lower-case letters. Then for each set of carbons give the 5 value and # of carbons it represents. letter δ value # of carbonsarrow_forwardarrow_back_iosSEE MORE QUESTIONSarrow_forward_ios
- Organic And Biological ChemistryChemistryISBN:9781305081079Author:STOKER, H. Stephen (howard Stephen)Publisher:Cengage Learning,General, Organic, and Biological ChemistryChemistryISBN:9781285853918Author:H. Stephen StokerPublisher:Cengage LearningIntroduction to General, Organic and BiochemistryChemistryISBN:9781285869759Author:Frederick A. Bettelheim, William H. Brown, Mary K. Campbell, Shawn O. Farrell, Omar TorresPublisher:Cengage Learning
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