• 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
Organic Chemistry Chem 121: Topics
Organic Chemistry Chem 121: Topics

... 1. Notice that methyl itself is not considered. 2. Notice the number of H atoms: 1o= 2H; 2o= 1H; 3o= 0 3. This distinction is not limited to halides, but applies to all sp3 hybridized carbon atoms with a substituent, eg. –OH (alcohols), etc. 4. For non-substituted C atoms an H atom replaces the subs ...
effective: september 2003 curriculum guidelines
effective: september 2003 curriculum guidelines

... Calendar Description: This is part two of a comprehensive second year organic chemistry course suitable for those majoring in chemistry/biochemistry or continuing on with studies in the Health Sciences. It begins with a review of the theory behind various spectroscopic methods of structure determina ...
Chem 30BL_Lecture 2_.. - UCLA Chemistry and Biochemistry
Chem 30BL_Lecture 2_.. - UCLA Chemistry and Biochemistry

... • Catalytic reduction of an alkyne i.e., Lindlar catalyst (Pd) to form cis-alkenes, Na/NH3(l) to form trans-alkenes • Wittig reaction (R’R”C=PR3) from an aldehyde or ketone • Tebbe’s reagent ((C5H5)2Ti(m2-CH2)(m2-Cl)Al(CH3)2) from an ...
Part (d) The Birch Reduction of Nitrogen
Part (d) The Birch Reduction of Nitrogen

... When nucleophiles attack the C=O group they do so by passing electrons from their highest occupied molecular orbital (HOMO) to the lowest unoccupied molecular orbital (LUMO) of the carbonyl ie. Negatively charged species are also attracted to the electron deficient carbon atom. So, in the addition ...
10. Alkyl Halides - faculty at Chemeketa
10. Alkyl Halides - faculty at Chemeketa

... 10. Organohalides ...
Chapter 7 - people.vcu.edu
Chapter 7 - people.vcu.edu

... o 2n+2+(number of N)-(number of X)  Note: This is different than the way Mr. Baker and the book do it, so be careful not to blend the two methods.  I just think this way is easier.  2) Subtract the “actual hydrogen” o Note: If you’re using the formula in step one, you do not add the halogens to t ...
Chapter 18 lectures as pdf
Chapter 18 lectures as pdf

... • Primary amines – imines if water removed • Secondary amines – enamines if water removed ...
Chem 30BL * Lecture 2 - UCLA Chemistry and Biochemistry
Chem 30BL * Lecture 2 - UCLA Chemistry and Biochemistry

... • Catalytic reduction of an alkyne i.e., Lindlar catalyst (Pd) to form cis-alkenes, Na/NH3(l) to form trans-alkenes • Wittig reaction (R’R”C=PR3) from an aldehyde or ketone • Tebbe’s reagent ((C5H5)2Ti(m2-CH2)(m2-Cl)Al(CH3)2) from an ...
الشريحة 1 - Systematic Approach to Teaching
الشريحة 1 - Systematic Approach to Teaching

... • Alcohols are prepared:From alkene by hydration, 2) From alkyl halide by SN using aqueous NaOH, 3) From aldehydes or ketones by reduction using NaBH4 or Li Al H4. & 4) From Acids or esters by reduction using Li Al H4. • * Amines are prepared from alkyl halides using NH3 or NaNH2. • * Amines could b ...
Demonstrate skill in organic chemistry techniques.
Demonstrate skill in organic chemistry techniques.

... Discuss the physical properties of alcohols and summarize the methods used to synthesize them. Learning Objectives Draw structures and name alcohols, phenols, diols, and thiols. Predict relative boiling points, acidities, and solubilities. Show the conversion of alcohols from alkenes, alkyl halides, ...
chemistry 30 / unit c chemical changes of organic compounds
chemistry 30 / unit c chemical changes of organic compounds

... ( carbonates,cyanides, carbides, and oxides of carbon ) K.2 Identify and describe significant organic compounds in daily life: demonstrating generalized knowledge of their origins and applications(eg. methane,methanol,ethane,ethanol,ethanioic acid,propane,benzene,octane glucose, polyethylene . K.3 N ...
Topic 12: Organic Chemistry
Topic 12: Organic Chemistry

... with 3 carbon atoms ...
Organic Molecules
Organic Molecules

... The Cycloalkanes If the carbon chain that forms the backbone of a straight-chain hydrocarbon is long enough, we can envision the two ends coming together to form a cycloalkane. One hydrogen atom has to be removed from each end of the hydrocarbon chain to form the C C bond that closes the ring. Cycl ...
Chapter 11
Chapter 11

... Therefore often need to add an additional Lewis acid to convert an alcohol to alkyl chloride (even with 2˚ and 3˚ alcohols that proceed through SN1) ...
organic chem - WordPress.com
organic chem - WordPress.com

... Dec- ...
Ester Lab / Adobe Acrobat Document
Ester Lab / Adobe Acrobat Document

... amber dichromate ion to the green chromium(III) can be quantitatively interpreted to determine blood alcohol (ethanol) levels. Second generation breathalyzer tests measure the amount of water produced in the reaction, for a more accurate measure. Secondary alcohols (OH attached to a non-terminal car ...
Aldehydes, Ketones and Carboxylic Acids
Aldehydes, Ketones and Carboxylic Acids

... • Can aldehydes and ketones set up hydrogen bonds with each other? • Can they set them up with water? ...
Chemistry
Chemistry

... concept of Armaticity; Huckel Rule. Electrophilic substitution reactions. Orientation and reactivity. Applications in Synthesis; Oxidat6ion of side Chain of aromatic hydrocarbons; Elementary treatment of aromaticity of pyridine and comparison of its reactivity with that of benzene. A brief introduct ...
Ch13 Lecture
Ch13 Lecture

... Nomenclature of Alkenes and Alkynes • When naming cycloalkenes, the double bond is located between C1 and C2. • The “1” is usually omitted in the name. • The ring is numbered to give the first substituent the lower number. ...
NCEA Level 2 Chemistry (91165) 2014
NCEA Level 2 Chemistry (91165) 2014

... When propanamine reacts with HCl or H2SO4, acid-base reactions occur. Amines are bases and as a result amines accept protons from acids. In these two reactions both sulfuric acid and hydrochloric acid donate protons to the amine to form organic salts. When propan-1-ol reacts with HCl, a substitution ...
WHAT IS MORPHINE -- ACTIVITY #1 What is morphine? What is it
WHAT IS MORPHINE -- ACTIVITY #1 What is morphine? What is it

Bulent Terem - CH324 - Syllabus | Chaminade
Bulent Terem - CH324 - Syllabus | Chaminade

...  Understand the basic principles of infrared and nuclear magnetic resonance spectroscoscopy, as well as mass spectrometry as tools to determine structures of organic molecules.  Learn to develop synthetic strategies based on carbonyl group chemistry in an effort to propose regioselective multi-ste ...
Whitten, Davis, and Peck, General Chemistry, 6th Edition
Whitten, Davis, and Peck, General Chemistry, 6th Edition

... Recommended CER Experiments to accompany Hornback’s Organic Chemistry, Second Edition The table below matches sections from the book with recommended CER labs. Click on the experiment title to view a PDF of each lab. Go to www.CERLabs.com to search the complete CER database and to learn more about c ...
a guide to 1h nmr chemical shift values
a guide to 1h nmr chemical shift values

... Hydrogen nuclei themselves possess a small magnetic field, and can influence the signal seen for hydrogens on neighbouring carbon atoms. This is known as spin-spin coupling. The number of signals the original signal is split into is equal to the number of hydrogens on neighbouring carbon atoms plus ...
Organic Reactions Worksheet
Organic Reactions Worksheet

... iv) Write the balanced equation for each oxidizing reaction, use [O] convention c. Using any secondary alcohol: i) Give the displayed (structural formula) which it could be oxidized to ii) State which homologous series the products are part of iii) Write the balanced equation for each oxidizing reac ...
< 1 ... 114 115 116 117 118 119 120 121 122 ... 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