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Exam 1 from 2008
Exam 1 from 2008

... a) Draw an accurate 3D structure of allene. (Hint: It is not planar.) On this structure show the p-orbitals and how they overlap to form the pi bonds in allene. Clearly indicate the 3D orientation of the p-orbitals relative to the atoms in the molecule and to each other. b) Label the hybridization o ...
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Edexcel GCE - The Student Room
Edexcel GCE - The Student Room

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Exp 19 - Diphenylacetylene_2015

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... chain groups of the protein are titrated? Explain. 5. Explain the following observation. A rule of thumb is that a chemical reaction will go twice as fast for every 10o rise in temperature. This is true for enzymes up to a certain temperature at which point the reaction no longer occurs. 6. Assuming ...
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슬라이드 1
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... Isotope effects indicate that the collapse of the adduct by reductive elimination is the rate determining step. The more easily reduced, the more reactive is the compound toward cuprate reagents. Compounds such as a,b-unsaturated esters and nitriles, which are not as easily reduced as the correspond ...
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... alcohol or the acid can be used in excess. The choice can be based on cost, availability and/or ease of purification at the end of the reaction. In this reaction we will add an excess of the acid. Sulfuric acid (H2SO4) is used as a catalyst for this reaction in order to accelerate the rate at which ...
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Lecture Resource ()

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Practice Test 2

... Vinegar contains a weak acid, acetic acid (HC2H3O2), which is responsible for its acidity. In one analysis of a commercial vinegar brand, a 15.0 mL sample was titrated with 0.4500 M NaOH. It required 30.50 mL of this NaOH solution to neutralize the acid in the vinegar sample. What is the molar conce ...
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Organic Pathways

... liquids are separated by what can be considered to be a succession of simple distillations. • When the mixture of liquids is heated in the distillation flask, the vapours rise up the fractioning column. • These vapours contain a higher concentration of the more volatile component than the liquid in ...
Second Semester Final Review Guide
Second Semester Final Review Guide

... 4. The substance containing the element that causes another element to gain electrons is called what? a. Oxidizing agent ...
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Hofmann–Löffler reaction



The Hofmann–Löffler reaction (also referred to as Hofmann–Löffler–Freytag reaction, Löffler–Freytag reaction, Löffler–Hofmann reaction, as well as Löffler's method) is an organic reaction in which a cyclic amine 2 (pyrrolidine or, in some cases, piperidine) is generated by thermal or photochemical decomposition of N-halogenated amine 1 in the presence of a strong acid (concentrated sulfuric acid or concentrated CF3CO2H). The Hofmann–Löffler–Freytag reaction proceeds via an intramolecular hydrogen atom transfer to a nitrogen-centered radical and is an example of a remote intramolecular free radical C–H functionalization.
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