• 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
136KB - NZQA
136KB - NZQA

... Two products are formed in this reaction because propene is an asymmetric alkene. When another asymmetric molecule such as hydrogen chloride, HCl, is added to it, there are two possible products. One product is produced in greater quantities (the major product) than the other (minor product). The ru ...
Enantiospecific skeleton expanding cross
Enantiospecific skeleton expanding cross

... with an extremely cheap ZnCl2 catalyst, and high enantiospecificity render this reaction ideal for low cost organic synthesis. In just one example, a lactic acid derivative is converted to 2-methylhexanoic acid with excellent yield. This compound is an important building block in the production of t ...
The World of Chemistry
The World of Chemistry

... ...
Slide 1
Slide 1

... They are nonpolar molecules and consequently are not soluble in water but are soluble in typical nonpolar organic solvents like toluene or pentane. Hydrocarbons are constructed of chains or rings of carbon atoms with sufficient hydrogens to fulfill carbons need for four bonds. ...
Chem. Commun. 2005, 501-503.
Chem. Commun. 2005, 501-503.

... ...
Organic Nomenclature - Alkanes, Alkenes, Alkynes
Organic Nomenclature - Alkanes, Alkenes, Alkynes

... HW Functional Groups and Nomenclature Functional Groups and Nomenclature A functional group in an organic molecule is an atom or a group of atoms that replaces a hydrogen atom in a hydrocarbon. The R stands for the hydrocarbon that makes up the rest of the molecule. ...
SCH4C Organic Test
SCH4C Organic Test

... A) contain double bonds, while alkenes have only single bonds B) contain only single bonds, while alkenes have at least one double bond C) are very reactive, while alkenes are unreactive D) contain only single bonds, while alkenes have at least one triple bond ____ 17. Alkynes contain A) one or more ...
CH 12-3 Power Point
CH 12-3 Power Point

... Alkyl halides react with Mg metal in ether solvent to form the “Grignard Reagent” containing a coordinate covalent bond. The metal stabilizes the carbon-anion. ...
International Arab Baccalaureate
International Arab Baccalaureate

... acid and the appropriate amine, whereas in hydrolysis a molecule is cleaved into two parts by the addition of a molecule of water. Question 2: Amides can be hydrolyzed under acidic or basic conditions. Describe the reaction of hydrolysis and give the obtained compounds in acidic medium. ...
(substituted) carbon
(substituted) carbon

... Hydroboration-oxidation of alkenes allows stereospecific and regioselective synthesis of alcohols. The reaction sequence exhibits anti-Markovnikov regioselectivity which complements acid-catalyzed hydration and oxymercurationdemercuration. The reaction mechanism does not involve a carbocation and t ...
Modules 261 12th edition
Modules 261 12th edition

... Intermolecular Forces (Van der Waals Forces) - dipole –dipole forces - hydrogen bonds - Dispersion Forces Dipole-Dipole Forces Boiling Points Solubilities Guidelines for Water Solubility Summary of Attractive Electronic Forces Infrared Spectroscopy: An Instrumental Method for Detecting Functional Gr ...
4.5: Bonding in Alcohols and Alkyl Halides
4.5: Bonding in Alcohols and Alkyl Halides

... 4.4: Classes of Alcohols and Alkyl Halides - Alcohols and alkyl halides are classified as according to the degree of substitution of the carbon bearing the halogen or -OH group OH primary (1°) : one alkyl substituent secondary (2°) : two alkyl substituents tertiary (3°) : three alkyl substituents 2- ...
LOYOLA COLLEGE (AUTONOMOUS), CHENNAI – 600 034
LOYOLA COLLEGE (AUTONOMOUS), CHENNAI – 600 034

... 13. How is 1,3-butadien prepared? Give the reactions of 1,3-butadiene with a) maleic anhydride b) HBr. 14. Explain the mechanism of halogenation of alkane. 15. How will you prepare the following compounds from acetylene: a) acetaldehyde ...
N.b. A catalyst is a species which speeds up a chemical reaction but
N.b. A catalyst is a species which speeds up a chemical reaction but

... Chemistry Catalytic Addition of Hydrogen (Hydrogenation) Compare with the hydrogenation of alkanes H ...
AMIDES & AMINES
AMIDES & AMINES

... • Can be thought of as ammonia (NH3), with one, two or all three of its hydrogens substituted by alkyl groups • The number of substituted alkyl groups allow for primary (10), secondary (20), and tertiary (30) sub-classifications (similar to alcohols) ...
functional groups 1. PPT
functional groups 1. PPT

...  Alcohols are also considered to be either - primary, secondary, or tertiary alcohols  Designations correspond to which carbon atom the –OH group is bonded to - Affects Chemical Reactivity/Properties - Tertiary more reactive than Primary ...
Chapter 1 - chemistry
Chapter 1 - chemistry

... Organic reactions commonly involve the breaking of relatively strong covalent bonds. Catalysts are often needed. ...
Organic Chemistry
Organic Chemistry

... Alkenes and Alkynes Alkenes: hydrocarbons that contain a carboncarbon double bond. [CnH2n] CC=C ...
twelve important naval substances – bonding
twelve important naval substances – bonding

... as fuels or solvents. Most organic molecules consist of a structural backbone of C-C single bonds and one or more functional groups. Functional groups are portions of an organic molecule where carbon has bonds to atoms other than carbon or hydrogen. ...
sn2 reactions of alkyl halides
sn2 reactions of alkyl halides

... The reaction mixtures from this experiment should be collected in the labeled waste container. Do not put them down the drain. Ask your teaching assistant if you have any questions concerning the proper procedures for waste disposal. Part 1: Effect of Structure of the Alkyl Halide on the Relative Ra ...
Organic Chemistry
Organic Chemistry

... c. in reaction mechanisms, curly arrows show how electrons move – generally electrons from nucleophile move to electrophile 3. Low reactivity: Alkanes have low reactivity because they have nonpolar CC and CH bonds. But they can react. 4. High reactivity: a. Alkenes have pi bonds in which electrons a ...
Notes 07 Organometallic Compounds
Notes 07 Organometallic Compounds

... Compounds that contain _________________bond (______): Examples of M include ________(Grignard reagents), _____________. ____________ carbon: Reacts with _____________ carbon and forms a new _________________. Nomenclature: Similar naming to substituted metals (alkyl metals or alkyl metal halides). ...
91165 Organic Chemistry Cornell Notes.
91165 Organic Chemistry Cornell Notes.

... SUMMARY: Alkanes are non-polar molecules that are insoluble in water. Their m.pt and b,pt increase as the number of carbon atoms in the molecule increase. Their two most important chemical reactions are combustion reactions (complete and incomplete) and substitution reaction with orange ...
Alkenes - MsReenChemistry
Alkenes - MsReenChemistry

... Electron deficient with positive or partial positive charges Examples NO2+, H+, ...
C h e m g u i d e  ... ALCOHOLS:  REPLACING THE -OH GROUP BY A HALOGEN
C h e m g u i d e ... ALCOHOLS: REPLACING THE -OH GROUP BY A HALOGEN

... 1. a) Describe what you would see if you added a small amount of phosphorus(V) chloride to an alcohol. b) This can only be used as a test for an alcohol if you first eliminate other compounds which also contain an -OH group. Give two completely different examples of something which would react with ...
< 1 ... 157 158 159 160 161 162 163 164 165 ... 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