• Study Resource
  • Explore Categories
    • Arts & Humanities
    • Business
    • Engineering & Technology
    • Foreign Language
    • History
    • Math
    • Science
    • Social Science

    Top subcategories

    • Advanced Math
    • Algebra
    • Basic Math
    • Calculus
    • Geometry
    • Linear Algebra
    • Pre-Algebra
    • Pre-Calculus
    • Statistics And Probability
    • Trigonometry
    • other →

    Top subcategories

    • Astronomy
    • Astrophysics
    • Biology
    • Chemistry
    • Earth Science
    • Environmental Science
    • Health Science
    • Physics
    • other →

    Top subcategories

    • Anthropology
    • Law
    • Political Science
    • Psychology
    • Sociology
    • other →

    Top subcategories

    • Accounting
    • Economics
    • Finance
    • Management
    • other →

    Top subcategories

    • Aerospace Engineering
    • Bioengineering
    • Chemical Engineering
    • Civil Engineering
    • Computer Science
    • Electrical Engineering
    • Industrial Engineering
    • Mechanical Engineering
    • Web Design
    • other →

    Top subcategories

    • Architecture
    • Communications
    • English
    • Gender Studies
    • Music
    • Performing Arts
    • Philosophy
    • Religious Studies
    • Writing
    • other →

    Top subcategories

    • Ancient History
    • European History
    • US History
    • World History
    • other →

    Top subcategories

    • Croatian
    • Czech
    • Finnish
    • Greek
    • Hindi
    • Japanese
    • Korean
    • Persian
    • Swedish
    • Turkish
    • other →
 
Profile Documents Logout
Upload
alcohols, alkyl halides, and nucleophilic substitutions
alcohols, alkyl halides, and nucleophilic substitutions

... minutes and allow to cool to room temperature. Report the results in tabular form. PART C: REACTIVITY OF HALIDES TOWARD SILVER NITRATE. Silver nitrate in ethanol. In this part of the experiment you will test the reactivity of several alkyl halides under SN1 reaction conditions. Organic halides may r ...
Chapter 20 Amines-part 2
Chapter 20 Amines-part 2

... è Primary and secondary amines undergo N-oxidation, but useful products are not obtained because of side-reactions è Tertiary amines undergo clean N-oxidation ...
Mr. Farnworth
Mr. Farnworth

... bonded compound that contains CARBON • Carbon atoms form FOUR covalent bonds in organic compounds • Methane CH4 (Draw structure) • Carbon atoms have four valence electrons for bonding. Each of theses electrons forms a different C-H Bond ...
Chapter One: Molecular Structure
Chapter One: Molecular Structure

... reaction between ethers and epoxides with nucleophiles under acidic and basic conditions.  Predict the stereochemistry and optical activity of a product from an understanding of its mechanism of formation.  Propose a reaction or sequence of reactions to produce a target ether or epoxide in high yi ...
Key Practice Exam 3
Key Practice Exam 3

... 4. Rank in increasing order the boiling points trends you would expect for alcohols, alkanes, ketones and carboxylic acids. Provide rationale for your ranking. Carboxylic acid > alcohol > ketones > alkanes The ranking is based on the ability of these compounds to form hydrogen bonds (their attractiv ...
Organic and Biochemical Molecules 1. Compounds composed of
Organic and Biochemical Molecules 1. Compounds composed of

... (Hydrogens on carbons are replaced –one at a time – with another atom. Aromatics prefer substitution, to addition, because of the resonance stabilization provided by the double bond) Example: ...
Topic 3 – Chemical Structure and Bonding
Topic 3 – Chemical Structure and Bonding

... o Nitration of benzene followed by reduction using Sn/HCl o Substitution of a halogen by CN- to lengthen a carbon chain o Acylation of a benzene ring followed by reduction using LiAlH4 to give an alcohol ...
5-3 - U of L Class Index
5-3 - U of L Class Index

...  They are classified based on the carbon the halogen is attached to If the carbon is attached to one other carbon that carbon is primary (1o) and the alkyl halide is also 1o If the carbon is attached to two other carbons, that carbon is secondary (2o) and the alkyl halide is 2o If the carbon is ...
Document
Document

...  If the carbon is attached to two other carbons, that carbon is secondary (2o) and the alkyl halide is 2o  If the carbon is attached to three other carbons, the carbon is tertiary (3o) and the alkyl halide is 3o ...
Naming carbon compounds - gilmorecollegeyr11chemistry
Naming carbon compounds - gilmorecollegeyr11chemistry

... Saturated compounds • A saturated compound has no double or triple bonds. • In saturated linear hydrocarbons, every carbon atom is attached to two hydrogen atoms, except those at the ends of the chain, which have three hydrogen atoms. • In the case of saturated methane, four hydrogen atoms are atta ...
Topic 11 Organic Chemistry
Topic 11 Organic Chemistry

... 3. Give the structural formulas of the four isomers of molecular formula C4H9Cl. State the name of each one and classify it as primary, secondary, or tertiary. ...
COUPLING REACTIONS IN ORGANIC SYNTHESIS
COUPLING REACTIONS IN ORGANIC SYNTHESIS

... The addition of dihydrogen to Vaska's complex and other transition metals is a reversible reaction. The hydrogen can be released again if the reaction moves to the left in a reductive elimination. That reversibility makes transition metal compounds useful for hydrogen storage. Hydrogen gas is volumi ...
Document
Document

... change in the receptor site. Not produced by the body. An organic molecule containing a carbon atom with a + charge. Intermediates in the electrophilic addition reactions of alkenes. A carbon atom with 4 different atoms or groups of atoms attached. A reaction in which two molecules join together and ...
Organic Chemistry
Organic Chemistry

...  Structural formula- provides the number and types of atoms in a molecule & shows bonding arrangement of the atoms. ...
Substitution Rxns-a-Sn2-12-quesx
Substitution Rxns-a-Sn2-12-quesx

... Question Assuming the reaction below takes place by a concerted process, which mechanistic scheme is correct? ...
11. Oxidation of alcohols, hydrolysis of halogenoalkanes and
11. Oxidation of alcohols, hydrolysis of halogenoalkanes and

... reacting species (15 minutes) (a) Potassium dichromate(VI) in aqueous sulphuric acid oxidizes propan-1-ol to two different products depending upon the reaction conditions. Draw the full structural formula of each product and state the reaction conditions required. ...
WS Unit Review File
WS Unit Review File

... 28. In terms of pH, explain why lemons are more acidic that bananas and why lye is more basic than ammonia. 29. Explain why water is BOTH an ACID and a BASE. 30. Why are carbon compounds SO abundant? ...
Organic Chemistry - Snow College | It's SNOWing
Organic Chemistry - Snow College | It's SNOWing

... alkoxides) and in protic solvents are better nucleophiles (better than alkoxides since they don’t H bond) ...
Document
Document

... alcohols to participate in substitution or elimination reactions. ...
Calculating Percent Yield
Calculating Percent Yield

... The electrons from the C-H bond then move down to reform the pi bond and the very stable aromatic ring. ...
Chapter 11: Reactions at an sp3 Hybridized Carbon III
Chapter 11: Reactions at an sp3 Hybridized Carbon III

... • In this case, however, the stability of tertiary carbocation which results from H– shifting and substituting for CH3OH makes this reaction work with HCl • If tertiary carbocations can be formed then HCl is strong enough to cleave ethers ...
Biochemistry Carbon Compounds Supplement 1 Name: . Answer
Biochemistry Carbon Compounds Supplement 1 Name: . Answer

... Biochemistry Carbon Compounds Supplement 1 ...
OChem 1 Mechanism Flashcards Dr. Peter Norris, 2015
OChem 1 Mechanism Flashcards Dr. Peter Norris, 2015

... Transition state is described as being trigonal bipyramidal shape ...
Dehydration notes-1
Dehydration notes-1

... 1. Put 10 mL 2-methylcyclohexanol and 2 mL of 85% phosphoric acid in a 25 mL round bottom flask (as the stillpot) with boiling stones. 2. Setup a simple distillation: attach the stillhead, thermometer, condenser, adapter, and use a graduated cylinder as the receiver. 3. Heat slowly to 96 oC and main ...
Carbon Compounds
Carbon Compounds

... • Are compounds that contain only the elements carbon and hydrogen. • Properties of Hydrocarbons: 1. Hydrocarbons mix poorly with water 2. Hydrocarbons are flammable. Chemical Formulas of Hydrocarbons: ...
< 1 ... 150 151 152 153 154 155 156 157 158 ... 171 >

Haloalkane



The haloalkanes (also known, as halogenoalkanes or alkyl halides) are a group of chemical compounds derived from alkanes containing one or more halogens. They are a subset of the general class of halocarbons, although the distinction is not often made. Haloalkanes are widely used commercially and, consequently, are known under many chemical and commercial names. They are used as flame retardants, fire extinguishants, refrigerants, propellants, solvents, and pharmaceuticals. Subsequent to the widespread use in commerce, many halocarbons have also been shown to be serious pollutants and toxins. For example, the chlorofluorocarbons have been shown to lead to ozone depletion. Methyl bromide is a controversial fumigant. Only haloalkanes which contain chlorine, bromine, and iodine are a threat to the ozone layer, but fluorinated volatile haloalkanes in theory may have activity as greenhouse gases. Methyl iodide, a naturally occurring substance, however, does not have ozone-depleting properties and the United States Environmental Protection Agency has designated the compound a non-ozone layer depleter. For more information, see Halomethane. Haloalkane or alkyl halides are the compounds which have the general formula ″RX″ where R is an alkyl or substituted alkyl group and X is a halogen (F, Cl, Br, I).Haloalkanes have been known for centuries. Chloroethane was produced synthetically in the 15th century. The systematic synthesis of such compounds developed in the 19th century in step with the development of organic chemistry and the understanding of the structure of alkanes. Methods were developed for the selective formation of C-halogen bonds. Especially versatile methods included the addition of halogens to alkenes, hydrohalogenation of alkenes, and the conversion of alcohols to alkyl halides. These methods are so reliable and so easily implemented that haloalkanes became cheaply available for use in industrial chemistry because the halide could be further replaced by other functional groups.While most haloalkanes are human-produced, non-artificial-source haloalkanes do occur on Earth, mostly through enzyme-mediated synthesis by bacteria, fungi, and especially sea macroalgae (seaweeds). More than 1600 halogenated organics have been identified, with bromoalkanes being the most common haloalkanes. Brominated organics in biology range from biologically produced methyl bromide to non-alkane aromatics and unsaturates (indoles, terpenes, acetogenins, and phenols). Halogenated alkanes in land plants are more rare, but do occur, as for example the fluoroacetate produced as a toxin by at least 40 species of known plants. Specific dehalogenase enzymes in bacteria which remove halogens from haloalkanes, are also known.
  • studyres.com © 2026
  • DMCA
  • Privacy
  • Terms
  • Report