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those I choose is wrong please help Amides are formed from the reaction of carboxylic acids...
give the product(s) for the following reactions, and name all reactants and product Question 11 (1 point) What are the hydrolysis products of N-methylpropanamide? propanoic acid and methylamine propanoic acid, methylamine, and water O propanoic acid and ammonia Question 8 (1 point) ✓ Saved What are the products formed from the hydrolysis of methylpentanoate? methane and pentanoic acid methanol and pentanoic acid formic acid and pentanol O pentanal and water
Formation and Hydrolysis of Amides Identify the products by dragging the appropriate labels to their respective targets. Part A When acyl halides (R-COX) or acid anhydrides (R-OC-O-CO-R) react with primary amines (R-NH2) or secondary amines (R2 NH), the reaction yields an amide R-C-NR2 where R may be an alkyl group or hydrogen atom For example, propanoyl chloride |l reacts with ethanamine (CH3 CH2NH2) to form The IUPAC name for CH3 CH2C-Cl CH3 CH2C-NHCH2CHa the product is N-ethyl propanamide, as it...
Learning Goal: To predict the hydrolysis products of amides. In the presence of a strong acid, such as HCl, and amide reacts with water to produce a carboxylic acid and an ammonium or amine salt. In the presence of a strong base, like NaOH the amide reacts to produce ammonia or an amine, and a carboxylic acid salt. Draw the carboxylic acid product of the acid hydrolysis of methanamide, shown here. Figure | H C NHA Draw the molecule on...
Question 1 (0.5 points) Saved Proteins are formed by joining together. carboxylic acids fatty acids amino acids none of the above Question 2 (0.5 points) Which two functional groups does an amino acid contain? amine and carboxylic acid carboxylic acid and amide amide and heterocyclic ring heterocyclic ring and amine Question 3 (0.5 points) Do amino acids commonly exist in nature as neutral molecules with all uncharged atoms? Yes No Question 1 (0.5 points) What is a protein? A polymer...
1.) Please explain the importance of the Ficsher Esterfication reaction. 1-3 sentences will be sufficient. 2. Which one in more soluble in water, propanoic acid or 1,3-propanedioic acid? Please explain why? 1-2 sentences will be sufficient. 1.) Name all of the functional groups that can undergo hydrolysis, and give the corresponding products. Also, include any conditions per reaction. 2. What do carboxylic acids and carboxylic esters have in common in regards to reduction?
Need help with questions 2-4. Information: Just as it is beneficial to make a summary of the types of reactions, it is a list of the functional groups that commonly react by each of the Seven summary is shown in Table 2. is also useful to the ven pathways. Such reaction pathways Table 2: Functional groups that commonly react by the seven react acid-base - carboxylic acids, phenols (acids) - amines (bases) addition - alkenes, alkynes elimination - alcohols reduction...
Can someone help with the 4 POST LAB questions thanks Carboxylic Acids and Esters acid). like citric acid. Face crearboxyl the name implies, a Carbexylic Aclds A salad dressing made of The sour taste of fruits such as lemons is due to the presence of acids like citric acid. tcarboxyl a-hydroxy acids such functional group - that is, a carbonyl group attached to a hydroxyl group. AS dicarboxylic acid carboxylic acid of benzene is called benzoic acid (Figure 1). oil...
Questions and Problems 553 ation for the reaction that would produse cach of the following amines b. N.Methylpropanamine c. N.N-Diethylpentanamine 15.37 Briefly explain why the lower molar massamines (lewer than five carbons) exhibit appreciable solubility in water 15.38 Why is the salt of an amine appreciably more soluble in water than the mine from which it was formed 15.39 Most drugs containing amine groups are not administered as the mine but rather the amount you suggeste son why? 15.40 Why...
Carboxylic Acids and Esters EXPERIMENT 22 OBSERVATIONS AND RESULTS Synthesis and Identification of an Ester: Esterification 1. Give the name and structure of the ester which you synthesized. What fruit did you associate with the odor of the ester? to noldsoinogs w to esar bnn eaman sd vio stolpi Look up the ester and its fruit sburce in your textbook. (If it is not in your textbook, ask your instructor.) Did you associate the ester with the right fruit? If...
Read the description and choose the term that matches from the options in the list. A chemical species that is electron rich and may donate a pair of electrons to form a new covalent bond A compound where an intramolecular reaction between an aldehyde and an alcohol can occur A proteinaceous biological catalyst is an Choose... Hydrolysis Nucleotide Carbohydrate Electrophile Saponification protein Fatty acids Nucleophile Lipid nucleoside Enzyme peptide Condensation reaction A compound that is only extractable from biological material...