Draw the structure of the major organic product of the reaction. In those cases where there are two products, draw both. All carboxyl and amino groups should be drawn in the neutral form. о о NaOH H₂O Marvin JS- Troubleshooting Marvin JS- Compatibility S
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A: one is 'mu' and another is 'n' thank you
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- Consider the synthesis scheme in Figure 38. What type of compound is represented by C in the synthesis scheme? * Nitrile Carboxylic acid Acyl halide Ester AmideIdentify the ester product of the reaction. HC HC IU OT CH OH + MC- OH H+, heat HC HC. HC جدید IL HC. CH HC علام HC. CH CH | + H2O CH₂ CH₂ CH37. Strong base is added to the following structure/solution until the reaction is complete. Predict the odor of the NEW product formed /after the reaction has reached completion. Give the name of the reaction. H. H-C-C H. OH OA Sweet smelling Esterification OB. Unpleasant smell; Acid hydrolysis OC Pungent odor; Reduction of carboxylic acids O D. No odor, Neutralization
- Predict the Product. Predict the major organic product(s) or reactant(s) for the following reactions. HO Fr Iz NaOH, H₂O, heat NaOH, H₂O, heatThe amino acid phenylalanine can be made in the laboratory. Choose the correct reagents needed to make this molecule. NH3 (This zwitterionic form is common in aqueous solution) 1) PB13, Br2 , H2O 2) NaOH 3) NH3 1) PB13 , Br2, H20 2) NH3 3) H,О 1) НBг 2) LDA 3) NH3 1) NaOH 2) Br2 3) NH3Shown below is the structure of the fatty acid, lauric acid. H3C CH₂ _CH 2 CH2 CH2 CH 2 CH₂ CH2 CH₂ CH2 OH CH₂ C The boxed portion is considered to be both Opolar and hydrophilic Ohydrophilic and hydrophobic Opolar and hydrophobic nonpolar and hydrophilic nonpolar and hydrophobic
- 5. Write the products for the complete hydrolysis of: NH2 LOH H2N H. HOTrue or false The hydroxyl group found in an organic compound is responsible for its basicity. Aromatic hydrocarbons are considered polar and has high affinity to water. Acidic drugs are a class of chemical compounds that normally have high hydrophilicity and negative charges. Amino groups attached to hydrocarbons are considered polar which may be responsible for its solubility. Lipophilic drugs have a faster rate of absorption than hydrophilic drugs.Complete the following reactions by providing missing reactants or products as appropriate.
- List the requested biological classification or organic functional group(s) for the reactant(s) first , predict the reaction type, and predict the product(s) classification or functional group(s). Use the information to draw the major product(s)Draw the structure of the product that forms when the carbonyl compound shown is treated with K,Cr₂O, If no reaction occurs, draw the structure of the organic starting material (reactant). CH,(CH,), (CO)CH(CH,), Click and drag to start drawing a structure. 1 :0 Statover G 0Identify the reaction type. a. acid base b. dehydration c. hydration d. amide synthesis e. hydrolysis (in base) f. esterification g. hydrolysis (in acid)