(a)
Interpretation:
Compounds with wrong names are given. Correct name for each compound is to be stated.
Concept introduction:
IUPAC has established rules to name an organic compound. Any organic compound has only one name that denotes that compound. The root word determines the number of carbons while counting the longest carbon chain. Double or triple bond should be given lowest carbon number. Whenever possible, the substituent should get lowest number. If more than one substituent is present, prefixes like di, tri, tetra, etc. are used.
(b)
Interpretation:
Compounds with wrong names are given. Correct name for each compound is to be stated.
Concept introduction:
IUPAC has established rules to name an organic compound. Any organic compound has only one name that denotes that compound. The root word determines the number of carbons while counting the longest carbon chain. Double or triple bond should be given lowest carbon number. Whenever possible, the substituent should get lowest number. If more than one substituent is present, prefixes like di, tri, tetra, etc. are used.
(c)
Interpretation:
Compounds with wrong names are given. Correct name for each compound is to be stated.
Concept introduction:
IUPAC has established rules to name an organic compound. Any organic compound has only one name that denotes that compound. The root word determines the number of carbons while counting the longest carbon chain. Double or triple bond should be given lowest carbon number. Whenever possible, the substituent should get lowest number. If more than one substituent is present, prefixes like di, tri, tetra, etc. are used.
(d)
Interpretation:
Compounds with wrong names are given. Correct name for each compound is to be stated.
Concept introduction:
IUPAC has established rules to name an organic compound. Any organic compound has only one name that denotes that compound. The root word determines the number of carbons while counting the longest carbon chain. Double or triple bond should be given lowest carbon number. Whenever possible, the substituent should get lowest number. If more than one substituent is present, prefixes like di, tri, tetra, etc. are used.
Trending nowThis is a popular solution!
Chapter 22 Solutions
OWLv2 with MindTap Reader, 4 terms (24 months) Printed Access Card for Zumdahl/Zumdahl's Chemistry, 9th
- 5. A solution of sucrose is fermented in a vessel until the evolution of CO2 ceases. Then, the product solution is analyzed and found to contain, 45% ethanol; 5% acetic acid; and 15% glycerin by weight. If the original charge is 500 kg, evaluate; e. The ratio of sucrose to water in the original charge (wt/wt). f. Moles of CO2 evolved. g. Maximum possible amount of ethanol that could be formed. h. Conversion efficiency. i. Per cent excess of excess reactant. Reactions: Inversion reaction: C12H22O11 + H2O →2C6H12O6 Fermentation reaction: C6H12O6 →→2C2H5OH + 2CO2 Formation of acetic acid and glycerin: C6H12O6 + C2H5OH + H₂O→ CH3COOH + 2C3H8O3arrow_forwardShow work. don't give Ai generated solution. How many carbons and hydrogens are in the structure?arrow_forward13. (11pts total) Consider the arrows pointing at three different carbon-carbon bonds in the molecule depicted below. Bond B 2°C. +2°C. cleavage Bond A •CH3 + 26.← Cleavage 2°C. + Bond C +3°C• CH3 2C Cleavage E 2°C. 26. weakest bond Intact molecule Strongest 3°C 20. Gund Largest argest a. (2pts) Which bond between A-C is weakest? Which is strongest? Place answers in appropriate boxes. C Weakest bond A Produces Most Bond Strongest Bond Strongest Gund produces least stable radicals Weakest Stable radical b. (4pts) Consider the relative stability of all cleavage products that form when bonds A, B, AND C are homolytically cleaved/broken. Hint: cleavage products of bonds A, B, and C are all carbon radicals. i. Which ONE cleavage product is the most stable? A condensed or bond line representation is fine. 13°C. formed in bound C cleavage ii. Which ONE cleavage product is the least stable? A condensed or bond line representation is fine. • CH3 methyl radical Formed in Gund A Cleavage c.…arrow_forward
- Chemistry & 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 LearningChemistry: An Atoms First ApproachChemistryISBN:9781305079243Author:Steven S. Zumdahl, Susan A. ZumdahlPublisher:Cengage Learning
- Introductory Chemistry: An Active Learning Approa...ChemistryISBN:9781305079250Author:Mark S. Cracolice, Ed PetersPublisher:Cengage LearningWorld of Chemistry, 3rd editionChemistryISBN:9781133109655Author:Steven S. Zumdahl, Susan L. Zumdahl, Donald J. DeCostePublisher:Brooks / Cole / Cengage LearningChemistry for Today: General, Organic, and Bioche...ChemistryISBN:9781305960060Author:Spencer L. Seager, Michael R. Slabaugh, Maren S. HansenPublisher:Cengage Learning