Chapter 17: Q50P (page 567)
What products would you expect to obtain from reaction of 1-methylcyclohexanol with the following reagents?
(a) HBr (b) NaH (c) H2SO4 (d) Na2Cr2O7
Chapter 17: Q50P (page 567)
What products would you expect to obtain from reaction of 1-methylcyclohexanol with the following reagents?
(a) HBr (b) NaH (c) H2SO4 (d) Na2Cr2O7
All the tools & learning materials you need for study success - in one app.
Get started for freeQuestion: Give IUPAC names for the following compounds:
TMS ethers can be removed by treatment with fluoride ion as well as by acid-catalyzed hydrolysis. Propose a mechanism for the reaction of cyclohexyl TMS ether with LiF. Fluorotrimethylsilane is a product.
Benzyl chloride can be converted intobenzaldehyde by treatment with nitromethane and base. The reactioninvolves the initial conversion of nitromethane in to its anion, followed by SN2 reaction of the anion with benzyl chloride and subsequent E2 reaction. Write the mechanism in detail, using curved arrows to indicate the electron flow in each step.
Benzyl chloride Nitromethane anion Benzaldehyde
Question:The trimethylsilyl (TMS) protecting group is one of several silicon protecting groups for alcohols. For each reaction, draw the mechanism for the protection of (R)-3-bromo-1-butanol with the following silyl chlorides, using triethylamine as the base:
(a) tert-butyldimethylsilyl chloride (TBS-Cl)
(b) triisopropylsilyl chloride (TIPS-Cl)
(c) triethylsilyl chloride (TES-Cl)
A compound of unknown structure gave the following spectroscopic data:
Mass spectrum:
IR:
NMR: 1.4 (2H, quartet, J=7Hz); 1.2 (6H, singlet); 1.0 (1H, singlet); 0.9 (3H, triplet, J=7Hz)
NMR: 74, 35, 27, 25
(a) Assuming that the compound contains C and H but may or may not contain O, give three possible molecular formulas.
(b) How many protons (H) does the compound contain?
(c) What functional group(s) does the compound contain?
(d) How many carbons does the compound contain?
(e) What is the molecular formula of the compound?
(f) What is the structure of the compound?
(g) Assign peaks in the molecule’s NMR spectrum corresponding to specific protons.
What do you think about this solution?
We value your feedback to improve our textbook solutions.