Concept explainers
(a)
Interpretation:
The condensed formula of the product of the reaction of ethylene glycol with stearic acid has to be drawn.
Concept Introduction:
Preparation of Esters:
Esters are prepared from the reaction of
The general preparation of esters is shown below,
Condensed formula: Condensed formula shows the arrangement of atoms in grouped form.
(b)
Interpretation:
The condensed formula of the product of the esterification reaction of oxalic acid with ethanol has to be drawn.
Concept Introduction:
Refer to part (a).
(c)
Interpretation:
The condensed formula of the product of the esterification reaction of 1-butanol with propanoic acid has to be drawn.
Concept Introduction:
Refer to part (a).
Want to see the full answer?
Check out a sample textbook solutionChapter 11 Solutions
ACHIEVE/CHEMICAL PRINCIPLES ACCESS 1TERM
- An alcohol is oxidized to a carboxylic acid, and 0.2003 g of the acid is titrated with 45.25 mL of 0.03811 M NaOH.(a) What is the molar mass of the acid? (b) What are the molarmass and molecular formula of the alcohol?arrow_forwardDraw the organic product formed when the following compounds undergo a substitution reaction: (a) acetic acid and 1-hexanol; (b) propanoic acid and dimethyl-amine; (c) ethanoic acid and diethylamine.arrow_forward5) Provide complete and balanced chemical reactions for the following. Write the formula and the name of the alcohol that when dehydrated, gives rise to the following alkenes. Give complete reactions. (а) СH-CH,CH-CH-CHCH-CHa (b) • 3-ethyl-1-hexanol is a primary alcohol. Give the two complete oxidation reactions using potassium permanganate.arrow_forward
- 5. Give the structural formulae and name the functional groups of the following compounds. (a) 3-chlorobut-1-ene (b) butanedioic acid Name the functional group: (c) propanamide Name the functional group: (d) 3-methylbutanal Name the functional group: Name the functional group:arrow_forward(b) Differentiate between bioethanol and biodiesel.arrow_forward(1) Write a complete chemical equation showing reactants, products, and catalysts needed (if any) for the following reaction and (2) Draw and name the organic compound found in every reaction. (a) Complete hydrogenation of 2-Methylhexa-1,5-diene (b) Complete halogenation (Br2) of 3-Ethyl-2,2-dimethylhept-3-ene (c) Reaction of (4E)-2.4-Dimethylhexa-1,4-diene with a mole of water (d) Reaction of cis-3,3-Dimethyl-4-propylocta-1,5-diene with two mole of HBr (e) Reaction of trans-1-Bromo-3-chlorocyclopentane with potassium hydroxide (f) Formation of Gilman reagent using isopropyl bromide (g) Ozonolysis of 3,3-Dimethyloct-4-yne (h) Complete halogenation (Cl2) of 3-Ethyl-5-methyl-1,6,8-decatriyne (i) Partial hydrogenation using Lindlar's Catalyst 2,2,5,5-Tetramethylhex-3-yne (i) Reaction of 3.4-Dimethylcyclodecyne with sodium amidearrow_forward
- Draw the organic product formed when the following compounds undergo a substitution reaction: (a) acetic acid and methyl-amine; (b) butanoic acid and 2-propanol; (c) Formica acid and 2-methyl-1-propanol.arrow_forwardWrite the condensed structural formula for each of thefollowing compounds: (a) 2-ethyl-1-hexanol, (b) methylphenyl ketone, (c) para-bromobenzoic acid, (d) butyl ethylether, (e) N,N-dimethylbenzamide.arrow_forwardWhat is the structure of the alcohol produced when 3-methyl-1-pentene undergoes (a) acid catalyzed hydration (b) oxymercuration/demercuration (c) hydroboration/oxidationarrow_forward
- Write a balanced equation for the incomplete combustion of each alkane: (a) CH 3CH 2CH 3; (b) CH 3CH 2CH 2CH 3.arrow_forwardWrite a complete chemical equation showing reactants, products, and catalysts needed (if any) for the following reaction and (2) Draw and name the organic compound found in every reaction.(Use condensed structural formula) (a) Complete hydrogenation of 2-Methylhexa-1,5-diene (b) Complete halogenation (Br2) of 3-Ethyl-2,2-dimethylhept-3-ene(c) Reaction of (4E)-2,4-Dimethylhexa-1,4-diene with a mole of waterarrow_forwardWrite balanced equations for the following reactions. Usestructural formulas to represent the organic compounds.(a) The complete combustion (to CO2 and H2O) of cyclopropanol(b) The reaction of isopropyl acetate with water to give acetic acid and isopropanol(c) The dehydration of ethanol to give ethene(d) The reaction of 1-iodobutane with water to give 1-butanolarrow_forward
- ChemistryChemistryISBN:9781305957404Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCostePublisher:Cengage LearningChemistryChemistryISBN:9781259911156Author:Raymond Chang Dr., Jason Overby ProfessorPublisher:McGraw-Hill EducationPrinciples of Instrumental AnalysisChemistryISBN:9781305577213Author:Douglas A. Skoog, F. James Holler, Stanley R. CrouchPublisher:Cengage Learning
- Organic ChemistryChemistryISBN:9780078021558Author:Janice Gorzynski Smith Dr.Publisher:McGraw-Hill EducationChemistry: Principles and ReactionsChemistryISBN:9781305079373Author:William L. Masterton, Cecile N. HurleyPublisher:Cengage LearningElementary Principles of Chemical Processes, Bind...ChemistryISBN:9781118431221Author:Richard M. Felder, Ronald W. Rousseau, Lisa G. BullardPublisher:WILEY