(a)
Interpretation:
Draw the possible structures of ethers with the molecular formula
Concept introduction:
Structural isomers are also called as constitutional isomers. These isomers can be defined as the molecules with same molecular formula and different structural formula. They are molecules in which the bonded atoms have different bonding with each other although the number of molecules is same. Identical molecules are molecules which have same structural formulae and same molecular formulae.
(b)
Interpretation:
Draw the possible structures of ethers with the molecular formula
Concept introduction:
Structural isomers are also called as constitutional isomers. These isomers can be defined as the molecules with same molecular formula and different structural formula. They are molecules in which the bonded atoms have different bonding with each other although the number of molecules is same. Identical molecules are molecules which have same structural formulae and same molecular formulae.
(c)
Interpretation:
Draw the possible structures of ethers with the molecular formula
Concept introduction:
Structural isomers are also called as constitutional isomers. These isomers can be defined as the molecules with same molecular formula and different structural formula. They are molecules in which the bonded atoms have different bonding with each other although the number of molecules is same. Identical molecules are molecules which have same structural formulae and same molecular formulae.
Want to see the full answer?
Check out a sample textbook solutionChapter 26 Solutions
General Chemistry: Principles and Modern Applications, Loose Leaf Version (11th Edition)
- Alcohols A, B and C all have the composition C4H 100. Molecules of alcohol A contain a branched carbon chain and can be oxidized to an aldehyde; molecules of alcohol B contain a linear carbon chain and can be oxidized to a ketone; and molecules of alcohol C can be oxidized to neither an aldehyde nor a ketone. Write the Lewis structures of these molecules.arrow_forward5. a) Draw two different structures with the molecular formula C2H6O. b) Name the functional group in each structure c)Which one will have the higher boiling point, and whyarrow_forward1. What is formed when a halogen molecule replaces hydrogen molecule(s) in an aromatic hydrocarbon? 2. What is formed when hydrogen molecules are replaced in an aliphatic hydrocarbon by halogen molecules? 3. What are a class of chemical compounds containing a hydroxyl group (-OH) bonded directly to an aromatic hydrocarbon group (like benzene)? 4. used to test for the presence of aromatic compounds in alcohols? 5. The dehydration of alcohols in the formation of ethers happens at _________.arrow_forward
- Acetyl chloride, CH3COCl, reacts with the hydroxyl groupsof alcohols to form ester groups with the elimination ofHCl. When an unknown compound X with formulaC4H8O3 reacted with acetyl chloride, a new compound Ywith formula C8H12O5 was formed.(a) How many hydroxyl groups were there in X?(b) Assume that X is an aldehyde. Write a possible structure for X and a possible structure for Y consistent with your structure for X.arrow_forward1. Explain the following - why stearic acid has higher melting point than decanoic acid. - why benzoic acid has higher melting point than stearic acid. - why salicylic acid has higher melting point than benzoic acid. - why octane has a higher melting point than isooctane. - why 2,2,3,3-tetramethylbutane has the highest melting point among the three isomers of C8H18.arrow_forwardThe melting points and boiling points of two isomeric alkanes are as follows: CH3(CH2)6CH3, mp = -57 °C and bp = 126 °C; (CH3)3CC(CH3)3, mp = 102 °C and bp = 106 °C. (a) Explain why one isomer has a lower melting point but higher boiling point. (b) Explain why there is a small difference in the boiling points of the two compounds, but a huge difference in their melting points.arrow_forward
- Chemistry: Principles and ReactionsChemistryISBN:9781305079373Author:William L. Masterton, Cecile N. HurleyPublisher:Cengage LearningChemistry & Chemical ReactivityChemistryISBN:9781337399074Author:John C. Kotz, Paul M. Treichel, John Townsend, David TreichelPublisher:Cengage LearningChemistry & Chemical ReactivityChemistryISBN:9781133949640Author:John C. Kotz, Paul M. Treichel, John Townsend, David TreichelPublisher:Cengage Learning
- Chemistry: Principles and PracticeChemistryISBN:9780534420123Author:Daniel L. Reger, Scott R. Goode, David W. Ball, Edward MercerPublisher:Cengage LearningChemistry by OpenStax (2015-05-04)ChemistryISBN:9781938168390Author:Klaus Theopold, Richard H Langley, Paul Flowers, William R. Robinson, Mark BlaserPublisher:OpenStaxChemistryChemistryISBN:9781305957404Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCostePublisher:Cengage Learning