Organic Reactions
... – Diatomic gas has two atoms – both add to opposite sides of the double bond (and opposite sides of the molecule) – Uses: Chlorine + ethane 1,2-dichloroethane: used as starting material for PVC – Uses: Br2 dissolved in dichloromethane is used to distinguish between alkenes and alkanes. If reddish- ...
... – Diatomic gas has two atoms – both add to opposite sides of the double bond (and opposite sides of the molecule) – Uses: Chlorine + ethane 1,2-dichloroethane: used as starting material for PVC – Uses: Br2 dissolved in dichloromethane is used to distinguish between alkenes and alkanes. If reddish- ...
Ethers - ThinkChemistry
... • The lower alcohols are miscible with water but as their chain length increases their solubility in water decreases. ...
... • The lower alcohols are miscible with water but as their chain length increases their solubility in water decreases. ...
Name - Clark College
... When electron density is shared through resonance, there is a greater extent of electron "sharing" than hyperconjugation. Since the electrons are shared by moving through like orbitals, the allylic radical is more stable. ...
... When electron density is shared through resonance, there is a greater extent of electron "sharing" than hyperconjugation. Since the electrons are shared by moving through like orbitals, the allylic radical is more stable. ...
Organic Functional Groups to know ASAP!
... Organic Functional Groups *The following organic functional groups will be studied throughout the course of the year: naming, physical/chemical properties, reactions, mechanisms, & synthesis. *Your first assignment is to become familiar (memorize) the following information so that you can easily wor ...
... Organic Functional Groups *The following organic functional groups will be studied throughout the course of the year: naming, physical/chemical properties, reactions, mechanisms, & synthesis. *Your first assignment is to become familiar (memorize) the following information so that you can easily wor ...
Organic Chemistry
... Contain 1 or more triple bonds “unsaturated” Not common in nature All 3 hydrocarbons have weak van der Waals forces—low boiling points Example C2H2 H—C=C—H Ethyne ...
... Contain 1 or more triple bonds “unsaturated” Not common in nature All 3 hydrocarbons have weak van der Waals forces—low boiling points Example C2H2 H—C=C—H Ethyne ...
Chemistry 212 Name:
... 5. Discuss the halogens. (5 points) Each halogen is obtained by oxidation of the halide ion to the halogen in a molten salt, except fluorine. None of the halogens is particularly abundant in nature, however all are easily accessible in concentrated forms rendering this point moot. All halogens have ...
... 5. Discuss the halogens. (5 points) Each halogen is obtained by oxidation of the halide ion to the halogen in a molten salt, except fluorine. None of the halogens is particularly abundant in nature, however all are easily accessible in concentrated forms rendering this point moot. All halogens have ...
Chem 263 Nov 3 2016 notes
... Many reactions of aldehydes and ketones start with nucleophilic attack at the carbon atom of the carbonyl group by a nucleophile (Nu:). The nucleophile always has a pair of electrons available but may or may not bear a negative charge. The electrons of the carbon-oxygen double bond then become loca ...
... Many reactions of aldehydes and ketones start with nucleophilic attack at the carbon atom of the carbonyl group by a nucleophile (Nu:). The nucleophile always has a pair of electrons available but may or may not bear a negative charge. The electrons of the carbon-oxygen double bond then become loca ...
dipole/induced-dipole and dipole/induced
... The reason for this behavior has to do with the very low polarizability of fluorine and a decrease in induced-dipole/induced-dipole forces that accompanies the incorporation of fluorine substituents into a molecule. Their weak intermolecular attractive forces give fluorinated hydrocarbons (fluorocar ...
... The reason for this behavior has to do with the very low polarizability of fluorine and a decrease in induced-dipole/induced-dipole forces that accompanies the incorporation of fluorine substituents into a molecule. Their weak intermolecular attractive forces give fluorinated hydrocarbons (fluorocar ...
Chapter 2: Alkanes Alkanes are molecules comprised of hydrogen
... with regards to electronic distribution, since electrons are continuously moving around the molecule, at any one time a molecule may have a small dipole moment (small polarization) causing nearby molecules to acquire small dipole moments. The resultant attractive force is dependent on the shared sur ...
... with regards to electronic distribution, since electrons are continuously moving around the molecule, at any one time a molecule may have a small dipole moment (small polarization) causing nearby molecules to acquire small dipole moments. The resultant attractive force is dependent on the shared sur ...
Primary, secondary and tertiary haloalkanes and
... Primary, secondary and tertiary haloalkanes and alcohols QUESTION: Answer the following questions on primary, secondary and tertiary haloalkanes and alcohols 1) Molecule 1 below can be classified as a tertiary alcohol. Molecule 2 can be classified as a tertiary haloalkane. ...
... Primary, secondary and tertiary haloalkanes and alcohols QUESTION: Answer the following questions on primary, secondary and tertiary haloalkanes and alcohols 1) Molecule 1 below can be classified as a tertiary alcohol. Molecule 2 can be classified as a tertiary haloalkane. ...
Primary, secondary and tertiary haloalkanes and alcohols
... Primary, secondary and tertiary haloalkanes and alcohols QUESTION: Answer the following questions on primary, secondary and tertiary haloalkanes and alcohols 1) Molecule 1 below can be classified as a tertiary alcohol. Molecule 2 can be classified as a tertiary haloalkane. ...
... Primary, secondary and tertiary haloalkanes and alcohols QUESTION: Answer the following questions on primary, secondary and tertiary haloalkanes and alcohols 1) Molecule 1 below can be classified as a tertiary alcohol. Molecule 2 can be classified as a tertiary haloalkane. ...
Carbon Chemistry
... ethyne (acetylene), a welding torch fuel. • Hydrocarbons that form rings of alternating double bonds between carbons are called “aromatics.” An example is benzene, a powerful solvent. ...
... ethyne (acetylene), a welding torch fuel. • Hydrocarbons that form rings of alternating double bonds between carbons are called “aromatics.” An example is benzene, a powerful solvent. ...
Addition reactions
... Electrophilic addition: an alkene or alkyne serves as the Nu: and donates : to the electropositive atom of a molecule, typically an acid • Substrate is unsaturated • Reactant is often an acid • The two halves (electropositive & electronegative) are both added “across” the double bond Nu:- ...
... Electrophilic addition: an alkene or alkyne serves as the Nu: and donates : to the electropositive atom of a molecule, typically an acid • Substrate is unsaturated • Reactant is often an acid • The two halves (electropositive & electronegative) are both added “across” the double bond Nu:- ...
ch08 by dr. Dina
... Hydration is favored by addition of a small amount of acid and a large amount of water Dehydration is favored by concentrated acid with very little water present (removal of water produced also helps favor dehydration) Carbocation rearrangements can occur ...
... Hydration is favored by addition of a small amount of acid and a large amount of water Dehydration is favored by concentrated acid with very little water present (removal of water produced also helps favor dehydration) Carbocation rearrangements can occur ...
Chapter 5 Summary - McGraw Hill Higher Education
... Alkenes and cycloalkenes contain carbon–carbon double bonds. According to IUPAC nomenclature, alkenes are named by substituting -ene for the -ane suffix of the alkane that has the same number of carbon atoms as the longest continuous chain that includes the double bond. The chain is numbered in the ...
... Alkenes and cycloalkenes contain carbon–carbon double bonds. According to IUPAC nomenclature, alkenes are named by substituting -ene for the -ane suffix of the alkane that has the same number of carbon atoms as the longest continuous chain that includes the double bond. The chain is numbered in the ...
WRL3502.tmp
... General Concepts Alkyl halides are most commonly synthesized from alcohols by replacing the hydroxyl group with a halide substituent. This is an example of nucleophilic aliphatic substitution, which is part of a very important group of reactions. The overall reaction is the same, but the mechanism v ...
... General Concepts Alkyl halides are most commonly synthesized from alcohols by replacing the hydroxyl group with a halide substituent. This is an example of nucleophilic aliphatic substitution, which is part of a very important group of reactions. The overall reaction is the same, but the mechanism v ...
Exam 1
... Determine reaction mechanisms from reaction outcome (see Mechanism work sheet). Be able to recognize the following functional groups: Aldehyde, Ketone, Carboxylic acid, ester, acid anhydride, amide and acyl halides (you do not have to know IUPAC naming) Know the relative reactivity’s of the carbonyl ...
... Determine reaction mechanisms from reaction outcome (see Mechanism work sheet). Be able to recognize the following functional groups: Aldehyde, Ketone, Carboxylic acid, ester, acid anhydride, amide and acyl halides (you do not have to know IUPAC naming) Know the relative reactivity’s of the carbonyl ...
Saturated Hydrocarbon
... Name of molecule: ___________________________________ Substituent: The halogens and groups of atoms including carbon, hydrogen, oxygen, nitrogen, sulfur, or phosphorus may take the place of a hydrogen atom attached to the parent chain. Alkyl group: A hydrocarbon substituent like methyl ─ CH3, ethyl, ...
... Name of molecule: ___________________________________ Substituent: The halogens and groups of atoms including carbon, hydrogen, oxygen, nitrogen, sulfur, or phosphorus may take the place of a hydrogen atom attached to the parent chain. Alkyl group: A hydrocarbon substituent like methyl ─ CH3, ethyl, ...
Alkanes - Warren County Schools
... 1) Aromatic- compounds with carbon and hydrogen that contain benzene rings 2) Aliphatic- compounds with carbon and hydrogen that are not aromatic (alkanes, alkenes, alkynes, and cycloalkanes) ...
... 1) Aromatic- compounds with carbon and hydrogen that contain benzene rings 2) Aliphatic- compounds with carbon and hydrogen that are not aromatic (alkanes, alkenes, alkynes, and cycloalkanes) ...
Document
... bromide to be less reactive than methyl bromide. Replacing all three hydrogen substituents by methyl groups almost completely blocks back-side approach to the tertiary carbon of (CH3)3CBr and shuts down bimolecular nucleophilic substitution. ...
... bromide to be less reactive than methyl bromide. Replacing all three hydrogen substituents by methyl groups almost completely blocks back-side approach to the tertiary carbon of (CH3)3CBr and shuts down bimolecular nucleophilic substitution. ...
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.