- 26.26.1: Draw the product of each coupling reaction. a. (CH2 CH)2CuLi Cl c. ...
- 26.26.2: Identify reagents A and B in the following reaction scheme. This sy...
- 26.26.3: Synthesize each product from the given starting materials using an ...
- 26.26.4: Draw the product of each reaction. a. + Pd(PPh3)4 NaOH O O I B b. B...
- 26.26.5: Synthesize each compound from the given starting materials. a. I CH...
- 26.26.6: Draw the coupling product formed when each pair of compounds is tre...
- 26.26.7: What starting materials are needed to prepare each compound using a...
- 26.26.8: Draw all stereoisomers formed when each alkene is treated with CHCl...
- 26.26.9: What reagents are needed to convert 2-methylpropene [(CH3)2C CH2] t...
- 26.26.11: What stereoisomers are formed when trans-3-hexene is treated with C...
- 26.26.12: Draw the products formed when each alkene is treated with Grubbs ca...
- 26.26.13: What products are formed when cis-2-pentene undergoes metathesis? U...
- 26.26.14: Draw the product formed from ring-closing metathesis of each compou...
- 26.26.15: When diene X is treated with Grubbs catalyst under high-dilution co...
- 26.26.16: What starting material is needed to synthesize each compound by a r...
- 26.26.17: Draw the products formed in each reaction. a. Cl (CH3CH2CH2) + 2CuL...
- 26.26.18: What organic halide is needed to convert lithium divinylcuprate [(C...
- 26.26.19: How can you convert ethynylcyclohexane to dienes AC using a Suzuki ...
- 26.26.21: In addition to organic halides, alkyl tosylates (R'OTs, Section 9.1...
- 26.26.22: What steps are needed to convert 1-butene (CH3CH2CH CH2) to octane ...
- 26.26.23: Draw the products (including stereoisomers) formed in each reaction...
- 26.26.24: Treatment of cyclohexene with C6H5CHI2 and Zn(Cu) forms two stereoi...
- 26.26.25: What ring-closing metathesis product is formed when each substrate ...
- 26.26.26: What starting material is needed to prepare each compound by a ring...
- 26.26.27: Metathesis reactions can be carried out with two different alkene s...
- 26.26.28: Draw the structure of the two products of molecular formula C15H26O...
- 26.26.29: When certain cycloalkenes are used in metathesis reactions, ring-op...
- 26.26.31: In addition to using CHX3 and base to synthesize dihalocarbenes (Se...
- 26.26.32: Draw a stepwise mechanism for the following reaction. CHBr2 Zn(Cu) ...
- 26.26.33: Sulfur ylides, like the phosphorus ylides of Chapter 21, are useful...
- 26.26.34: Although diazomethane (CH2N2) is often not a useful reagent for pre...
- 26.26.35: The reaction of cyclohexene with iodobenzene under Heck conditions ...
- 26.26.36: Devise a synthesis of diene A from (Z)-2-bromostyrene as the only o...
- 26.26.37: Devise a synthesis of (1E)-1-phenyl-1-hexene (CH3CH2CH2CH2CH CHPh) ...
- 26.26.38: Devise a synthesis of the given trans vinylborane, which can be use...
- 26.26.39: Devise a synthesis of each compound using a Heck reaction as one st...
- 26.26.41: Devise a synthesis of each compound from benzene. You may also use ...
- 26.26.42: Devise a synthesis of each substituted cyclopropane. Use acetylene ...
- 26.26.43: Biaryls, compounds containing two aromatic rings joined by a C C bo...
- 26.26.44: Draw the product formed from the ring-closing metathesis of each co...
- 26.26.45: Draw the product formed from the ring-closing metathesis of each co...
- 26.26.46: What reagents are needed to carry out transformations [1][3] in the...
- 26.26.47: Devise a synthesis of each of the following compounds. Besides inor...
- 26.26.48: Many variations of ring-closing metathesis have now been reported. ...
- 26.26.49: Suzuki coupling of aryl iodide A and vinylborane B affords compound...
Solutions for Chapter 26: CarbonCarbon Bond-Forming Reactions in Organic Synthesis
Full solutions for Organic Chemistry | 3rd Edition
ISBN: 9780077354725
Solutions for Chapter 26: CarbonCarbon Bond-Forming Reactions in Organic Synthesis
Get Full SolutionsThis expansive textbook survival guide covers the following chapters and their solutions. Chapter 26: CarbonCarbon Bond-Forming Reactions in Organic Synthesis includes 45 full step-by-step solutions. Organic Chemistry was written by and is associated to the ISBN: 9780077354725. Since 45 problems in chapter 26: CarbonCarbon Bond-Forming Reactions in Organic Synthesis have been answered, more than 221478 students have viewed full step-by-step solutions from this chapter. This textbook survival guide was created for the textbook: Organic Chemistry, edition: 3.
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1,2-elimination
An elimination reaction in which a proton from the beta (b) position is removed together with the leaving group, forming a double bond.
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amphoteric
Compounds that will react with either acids or bases. Amino acids are amphoteric.
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auxochrome
When applying Woodward-Fieser rules, the groups attached to the chromophore.
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base peak
In mass spectrometry, the tallest peak in the spectrum, which is assigned a relative value of 100%.
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closed system.
A system that enables the exchange of energy (usually in the form of heat) but not mass with its surroundings. (6.2)
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E2
A bimolecular eliminationreaction.eclipsed conformation (Sect. 4.7): A conformationin which groups are eclipsing each other in aNewman projection.
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endothermic
Any process with a positive DH (the system receives energy from the surroundings).
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Haworth projection
For substituted cycloalkanes, a drawing style used to clearly identify which groups are above the ring and which groups are below the ring. (See also Sect. 4.14.)
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Heat of reaction (DH0 )
The difference in enthalpy between reactants and products. If the enthalpy of products is lower than that of the reactants, heat is released and the reaction is exothermic. If the enthalpy of the products is higher than that of the reactants, energy is absorbed, and the reaction is endothermic
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Homotopic groups
Atoms or groups on an atom that give an achiral molecule when one of the groups is replaced by another group. The hydrogens of the CH2 group of propane, for example, are homotopic. Replacing either one of them with deuterium gives 2-deuteropropane, which is achiral. Homotopic groups have identical chemical shifts under all conditions
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ionic compound
A compound composed of cations and anions. (Section 2.7)
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Low-density lipoprotein (LDL)
Plasma particles, density 1.02–1.06 g/mL, consisting of approximately 26% proteins, 50% cholesterol, 21% phospholipids, and 4% triglycerides.
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Melt transition (Tm)
The temperature at which crystalline regions of a polymer melt.
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normal melting point
The melting point at 1 atm pressure. (Section 11.6)
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Pauli exclusion principle
No more than two electrons may be present in an orbital. If two electrons are present, their spins must be paired
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Polymer
From the Greek, poly 1 meros, meaning many parts. Any long-chain molecule synthesized by linking together many single parts called monomers
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reaction mechanism
A series of intermediates and curved arrows that show howthe reaction occurs in terms of the motion of electrons.
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Reductive elimination
Elimination of two substituents at a metal center, causing the oxidation state of the metal to decrease by two.
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Tautomers
Constitutional isomers in equilibrium with each other that differ in the location of a hydrogen atom and a double bond relative to a heteroatom, most commonly O, N, or S.
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tetrahedral
The geometry of an atom with four bonds separated from each other by 109.5°.