13. Write the chemical reaction for the base hydrolysis of each amide sample. Include the condensed structural formulas of the reactants and products. ACETAMIDE BENZAMIDE
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- Five examples each of organic acids, esters, amines, amides and alkaloids with their IUPAC name, structure, and uses.The hydrolysis of an amide in acidic conditions forms A. a carboxylate salt and an alcohol B. a carboxylate salt and an amine C. an alcohol and an amine salt (an ammonium ion) D. a carboxylic acid and an amine salt (an ammonium ion)Write two equations for the synthesis of each of the following amides. In one equation, use an acid chloride as areactant. In the second equation, use an acid anhydride.a. Ethanamideb. N-Propylpentanamidec. Propionamide
- 11. Write the chemical reaction for the acid hydrolysis of each amide sample. Include the 유 condensed structural formulas of the reactants and products. 11 CH3-C-NH₂ +H20+HCI CH3-C-OH + NH4+ CI- ACETAMIDE SO -NH2 +H20 T → 0 COOH + NH 3 11r Talking: Question 14.b of 25 Classify and describe the properties of the following nitrogen containing compound. Provide a systematic name for this structure. 2- N,N- 4- 1- tert- tri di sec- H N H. I N- N,N,N- n- prop but hex Submit +Benzoic acid reacts with ethylamine to form what kind of amide
- Complete this table for different amine compounds. Chemical propylamine quaternary ammonium ion methylphenylamine Molecular formula C3H9N C₂H7N C5H13N C4H10N Structural formula (CH3)3N (CH3)2NH CH 3 I (CH₂) 11 | H3C(CH2) 11 -N-(CH₂)11CH3 NHCH3 (CH₂)11 CH3 CH3CH2CH2-NH-CH3 + Classification Tertiary Quaternary Tertiary SecondaryWrite the names for the amines using the naming styles taught in the McMurry text. H2 H3C-N-C-CH3 name: H2 H2 H3C-C-Ņ-c-CH3 H name: These compounds are amines.What is an amide? What is its general formula? How do you classify an amide? Explain What makes amide prevalent in nature? Cite some amides found in our body. What are the properties of amide? What are the factors that affect these properties? Draw 5 amide structures and write their IUPAC name.
- Sketch the product, Then writeh the IUPAC NAME OF THE AMINE PRODUCT and the dominant Intermolecular force for the product. CH, NH, + H -CI O CH3-NH3*Cr, methylammonium chloride (Amine Product: H-Bond) O CH3-CH3-NH3*Cl', ethylammonium chloride (Amine Product: H-Bond) O CH3-NH3*, methylammonium ion (Amine Product: Dipole-Dipole) +. O CH3-NH3*CI , ethylammonium chloride (Amine Product: H-Bond) O CH3-NH3*CI', ethylammonium chloride (Amine Product: Dipole-Dipole) CH3-NH3*Cl", methylammonium chloride (Amine Product: lonic)Draw the products of acid–base reactions of aminesdraw the condensed structural formula for the product from the hydrolysis of each of the following amides with HCl
