Concept explainers
(a)
Interpretation:
The structure for each of the given thioesters.
Concept Introduction:
Thioesters are sulfur analogs of esters. The S-alkyl or S-aryl thioester has a carbonyl group and a sulfur-linked alkyl or aryl group. The first part of the name indicates that the alkyl or aryl group has bonded to the sulfur atom. The last part of the name indicates the
Answer to Problem 25.1P
Explanation of Solution
In the given name cyclohexyl thiobenzoate, the cyclohexyl is the alkyl group which is bonded to the sulfur atom. Thiobenzoate consists of a phenyl ring bonded to the sulfur atom through a carbonyl group. The structure for cyclohexyl thiobenzoate is drawn as below:
The structure for cyclohexyl thiobenzoate is:
(b)
Interpretation:
The structure for each of the given thioesters.
Concept Introduction:
Thioesters are sulfur analogs of esters. The S-alkyl or S-aryl thioester has a carbonyl group and a sulfur-linked alkyl or aryl group. The first part of the name indicates that the alkyl or aryl group has bonded to the sulfur atom. The last part of the name indicates the carboxylic acid stem. In common usage, the “S-“prefix is understood, and so, it is not mentioned.
Answer to Problem 25.1P
Explanation of Solution
The first part of the name suggests that the isopropyl group must be attached directly to the sulfur atom. The second part of the name suggests that the ester is formed from butanoic acid. In
The structure for S-isopropyl butanethioate is:
(c)
Interpretation:
The structure for each of the given thioesters.
Concept Introduction:
Thioesters are sulfur analogs of esters. The S-alkyl or S-aryl thioester has a carbonyl group and a sulfur-linked alkyl or aryl group. The first part of the name indicates that the alkyl or aryl group has bonded to the sulfur atom. The last part of the name indicates the carboxylic acid stem. In common usage, the “S-“prefix is understood, and so, it is not mentioned.
Answer to Problem 25.1P
Explanation of Solution
The first part of the name suggests that the phenyl ring must be attached directly to the sulfur atom. The second part of the name suggests that the ester is formed from the carboxylic acid which contains a cyclohexyl ring. In IUPAC nomenclature, “thio-“is inserted before the “ate” suffix in the name of the corresponding oxygen ester.
The structure for S-phenyl cyclohexanecarbothioate is shown as below:
The structure for S-phenyl cyclohexanecarbothioate is:
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Chapter 25 Solutions
Organic Chemistry, Ebook And Single-course Homework Access
- Calculate the voltage of each of the following cells. a) Fe(s)/Fe2+ (1.55 x 10-2 M)//Cu2+ (6.55 x 10-3 M)/Cu(s) b) Pt, H2 (0.255 bar)/HCl (4.55 x 10-4 M), AgCl (sat'd)/Ag Fe2+ +2e- = Fe E0= -0.44 V Cu2+ + 2e- = Cu E0= 0.337 V Ag+ + e- = Ag E0= 0.799 V AgCl(s) + e- = Ag(s) + Cl- E0= 0.222 V 2H+ + 2e- = H2 E0= 0.000 Varrow_forwardA solution contains 0.097 M Ce3+, 1.55x10-3 M Ce4+, 1.55x10-3 M Mn2+, 0.097 M MnO4-, and 1.00 M HClO4 (F= 9.649 x 104 C/mol). a) Write a balanced net reaction that can occur between species in this solution. b) Calculate deltaG0 and K for the reaction. c) Calculate E and deltaG for the conditions given. Ce4+ + e- = Ce3+ E0= 1.70 V MnO4- + 8H+ + 5e- = Mn2+ + 4H2O E0= 1.507 Varrow_forward1. Provide a step-by-step mechanism for formation of ALL STEREOISOMERS in the following reaction. Na HCO3 (Sodium bicarbonate, baking soda) is not soluble in CH2Cl2. The powder is a weak base used to neutralize strong acid (pKa < 0) produced by the reaction. Redraw the product to show the configuration(s) that form at C-2 and C-4. Br2 OH CH2Cl2 Na* HCO3 Br HO OH + Na Br +arrow_forward
- 2. Specify the solvent and reagent(s) required to carry out each of the following FGI. If two reagent sets must be used for the FGI, specify the solvent and reagent(s) for each reagent set. If a reaction cannot be carried out with reagents (sets) class, write NP (not possible) in the solvent box for reagent set #1. Use the letter abbreviation for each solvent; use a number abbreviation for reagent(s). Solvents: CH2Cl2 (A); H₂O (B); Reagents: HBr (1); R₂BH (6); H2SO4 (2); CH3OH (C); Br₂ (3); CH3CO₂H (D) NaHCO3 (4); Hg(OAc)2 (5); H₂O2/HO (7); NaBH4 (8) Reagent Set #1 Reagent Set #2 FGI + enant OH Solvent Reagent(s) Solvent Reagent(s)arrow_forwardGermanium (Ge) is a semiconductor with a bandgap of 2.2 eV. How could you dope Ge to make it a p-type semiconductor with a larger bandgap? Group of answer choices It is impossible to dope Ge and have this result in a larger bandgap. Dope the Ge with silicon (Si) Dope the Ge with gallium (Ga) Dope the Ge with phosphorus (P)arrow_forwardWhich of the following semiconductors would you choose to have photons with the longest possible wavelengths be able to promote electrons to the semiconductor's conduction band? Group of answer choices Si Ge InSb CdSarrow_forward
- Which of the following metals is the only one with all of its bands completely full? Group of answer choices K Na Ca Alarrow_forward2. Specify the solvent and reagent(s) required to carry out each of the following FGI. If two reagent sets must be used for the FGI, specify the solvent and reagent(s) for each reagent set. If a reaction cannot be carried out with reagents (sets) class, write NP (not possible) in the solvent box for reagent set #1. Use the letter abbreviation for each solvent; use a number abbreviation for reagent(s). Solvents: CH2Cl2 (A); Reagents: H₂O (B); CH3CO₂H (D) NaHCO3 (4); Hg(OAc)2 (5); HBr (1); R₂BH (6); H2SO4 (2); CH3OH (C); Br₂ (3); H₂O₂ / HO- (7); NaBH4 (8) Reagent Set #1 Reagent Set #2 FGI OH - α-α Br + enant Solvent Reagent(s) Solvent Reagent(s)arrow_forwardBased on concepts from Lecture 3-5, which of the following ionic compounds should be most soluble in water? Group of answer choices MgO BeO CaO BaOarrow_forward
- From an energy standpoint, which two process - in the correct order - are involved in the dissolving of an ionic compound crystal? Group of answer choices Water coordination to the ions followed by sublimation into the gas phase Sublimation of the crystal into gas-phase ions followed by water coordination to the ions Ion dissociation from the crystal followed by water coordination to the ions Water coordination to the ions followed by ion dissociation from the crystalarrow_forwardFor which Group 2 metal (M), is this process the most exothermic? M2+(g) + O2−(g) + CO2(g) → MO(s) + CO2(g) Group of answer choices M = Sr M = Mg M = Ca M = Baarrow_forward2. Specify the solvent and reagent(s) required to carry out each of the following FGI. If two reagent sets must be used for the FGI, specify the solvent and reagent(s) for each reagent set. If a reaction cannot be carried out with reagents (sets) class, write NP (not possible) in the solvent box for reagent set #1. Use the letter abbreviation for each solvent; use a number abbreviation for reagent(s). Solvents: CH2Cl2 (A); H₂O (B); Reagents: HBr (1); H2SO4 (2); CH3OH (C); Br₂ (3); CH3CO₂H (D) NaHCO3 (4); Hg(OAc)2 (5); R₂BH (6); H₂O₂ / HO- (7); NaBH4 (8) Reagent Set #1 Reagent Set #2 FGI Solvent Reagent(s) Solvent Reagent(s) HO OHarrow_forward
Organic ChemistryChemistryISBN:9781305580350Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. FootePublisher:Cengage Learning