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... • The reaction is called chlorination. This process is a substitution reaction, as a chlorine is substituted for a hydrogen . An analogous reaction, called bromination, occurs when the halogen source is bromine. ...
... • The reaction is called chlorination. This process is a substitution reaction, as a chlorine is substituted for a hydrogen . An analogous reaction, called bromination, occurs when the halogen source is bromine. ...
Functional Groups
... 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 (2 o) and the alkyl halide is 2o If the carbon is attached to three other carbons, the carbon is tertiary (3 o) and the a ...
... 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 (2 o) and the alkyl halide is 2o If the carbon is attached to three other carbons, the carbon is tertiary (3 o) and the a ...
Functional Groups
... 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 attached to three other carbons, the carbon is tertiary (3o) and the alk ...
... 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 attached to three other carbons, the carbon is tertiary (3o) and the alk ...
aldehyde,ketones and Haloalkanes
... Explain as to why haloarenes are much less reactive than haloalkanes towards nucleophilic substitution reactions. Which compound in each of the following pairs will react faster in SN2 reaction with – OH? Why? [3] (i) CH3Br or CH3I (ii) ...
... Explain as to why haloarenes are much less reactive than haloalkanes towards nucleophilic substitution reactions. Which compound in each of the following pairs will react faster in SN2 reaction with – OH? Why? [3] (i) CH3Br or CH3I (ii) ...
Hydrocarbons
... Combustion – Alcohols burn without producing soot or smoke (carbon) Oxidation – Primary alcohols can be oxidised to create carboxylic acids. We can use acidified dichromate or acidified permanganate as oxidising agents Elimination – As you might have guessed elimination reactions remove parts of the ...
... Combustion – Alcohols burn without producing soot or smoke (carbon) Oxidation – Primary alcohols can be oxidised to create carboxylic acids. We can use acidified dichromate or acidified permanganate as oxidising agents Elimination – As you might have guessed elimination reactions remove parts of the ...
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... using a large excess of concentrated acid (HCl and zinc chloride) • we can distinguish between 1°, 2° and 3° alcohols by their different rates of reaction using the Lucas Test • order of reactivity: – tertiary > secondary > primary ...
... using a large excess of concentrated acid (HCl and zinc chloride) • we can distinguish between 1°, 2° and 3° alcohols by their different rates of reaction using the Lucas Test • order of reactivity: – tertiary > secondary > primary ...
The Chemistry of Alkyl Halides - Welcome to people.pharmacy
... In a stereospecific reaction with a given stereochemistry—anti-elimination, in this case—a diastereomeric product requires a diastereomeric starting material (either enantiomer). The easiest path to the answer is to convert the starting material in Eq. 9.40a into its diastereomer by the interchange ...
... In a stereospecific reaction with a given stereochemistry—anti-elimination, in this case—a diastereomeric product requires a diastereomeric starting material (either enantiomer). The easiest path to the answer is to convert the starting material in Eq. 9.40a into its diastereomer by the interchange ...
- KCN K+ R KOH + H2O
... (hemiaminal) followed by E1 elimination of H2O. Note that this reaction requires the presence of at least two hydrogens in the starting amine (H+ comes from N; O is protonated before it leaves) ii) Equilibrium favors imine formation when R” = hydroxy, alkoxy, or amino groups; the products called oxi ...
... (hemiaminal) followed by E1 elimination of H2O. Note that this reaction requires the presence of at least two hydrogens in the starting amine (H+ comes from N; O is protonated before it leaves) ii) Equilibrium favors imine formation when R” = hydroxy, alkoxy, or amino groups; the products called oxi ...
Carboxylic Acid Derivatives
... A similar procedure is used to make amides from acyl chlorides and amines (the amine must have at least one hydrogen attached to the nitrogen). ...
... A similar procedure is used to make amides from acyl chlorides and amines (the amine must have at least one hydrogen attached to the nitrogen). ...
Chem 130 Fall 2004 Exam 3 Study Guide Chapter 8.1
... Chem 130 Fall 2004 Exam 3 Study Guide Chapter 8.1-8.4 – Alcohols 1. Nomenclature of Alcohols 2. Properties Hydrogen Bonding: boiling point 3. Reactions of Alcohols Conversion into alkyl halides (with HCl, HBr, SOCl2) Dehydration to form alkene (with H2SO4, concentrated, ∆) Oxidation: Primary ...
... Chem 130 Fall 2004 Exam 3 Study Guide Chapter 8.1-8.4 – Alcohols 1. Nomenclature of Alcohols 2. Properties Hydrogen Bonding: boiling point 3. Reactions of Alcohols Conversion into alkyl halides (with HCl, HBr, SOCl2) Dehydration to form alkene (with H2SO4, concentrated, ∆) Oxidation: Primary ...
Worksheet Key - UCSB C.L.A.S.
... 9. How many compounds can be produced if you mix chlorine with ethane in the presence of high energy photons? 9 monochlorination CH3CH2Cl dichlorination ClCH2CH2Cl or CH3CHCl2 trichlorination Cl2CHCH2Cl or CH3CCl3 tetrachlorination Cl2CHCHCl2 or ClCH2CCl3 pentachlorination Cl2CHCCl3 hexachlorination ...
... 9. How many compounds can be produced if you mix chlorine with ethane in the presence of high energy photons? 9 monochlorination CH3CH2Cl dichlorination ClCH2CH2Cl or CH3CHCl2 trichlorination Cl2CHCH2Cl or CH3CCl3 tetrachlorination Cl2CHCHCl2 or ClCH2CCl3 pentachlorination Cl2CHCCl3 hexachlorination ...
Document
... When naming alkenes we follow the same rules as for the alkanes with one major difference; • the main chain (the longest chain) must contain the double bond, whose position is indicated by a number. • The chain is numbered to make this number as small as possible (the double bond takes ...
... When naming alkenes we follow the same rules as for the alkanes with one major difference; • the main chain (the longest chain) must contain the double bond, whose position is indicated by a number. • The chain is numbered to make this number as small as possible (the double bond takes ...
Unit 8 – Organic Chemistry
... more reactive than alkanes – Since no hydrogen is lost, this reaction is called an addition reaction, and occurs at room temperature – Alkenes and alkynes will react with halogens, as well as hydrogen halides and water ...
... more reactive than alkanes – Since no hydrogen is lost, this reaction is called an addition reaction, and occurs at room temperature – Alkenes and alkynes will react with halogens, as well as hydrogen halides and water ...
Name: Chem 22 Final exam Spring `00 What product is formed when
... e) addtion of a hydride ion and a proton more or less at the same time 18. Which of the following describes “reductive amination?” a) an aldehyde or a ketone + a tertiary amine + H2/zeolite b) an aldehyde or a ketone + ammonia or a primary or a secondary amine + ...
... e) addtion of a hydride ion and a proton more or less at the same time 18. Which of the following describes “reductive amination?” a) an aldehyde or a ketone + a tertiary amine + H2/zeolite b) an aldehyde or a ketone + ammonia or a primary or a secondary amine + ...
Assignment 4 Task 1a
... have been assigned to a new case and are working as part of a team to solve the case. Working in the laboratory you will need to have a good understanding of the conventions adopted to ensure that all chemical compounds have unambiguous names. You also need to understand how a combination of element ...
... have been assigned to a new case and are working as part of a team to solve the case. Working in the laboratory you will need to have a good understanding of the conventions adopted to ensure that all chemical compounds have unambiguous names. You also need to understand how a combination of element ...
Organic Chemistry 25.2 Introduction to Hydrocarbons
... Hydrocarbons are relatively unreactive; for an organic molecule to be reactive it needs something additional. ...
... Hydrocarbons are relatively unreactive; for an organic molecule to be reactive it needs something additional. ...
Secondary alcohols
... Haloalkanes can be made from alcohols through inorganic esters. As an alternative to the acid-catalyzed conversions of alcohols into haloalkanes, a number of inorganic reagents can convert the alcoholic hydroxyl group into a good leaving group under milder conditions. Reaction of PBr3 with a second ...
... Haloalkanes can be made from alcohols through inorganic esters. As an alternative to the acid-catalyzed conversions of alcohols into haloalkanes, a number of inorganic reagents can convert the alcoholic hydroxyl group into a good leaving group under milder conditions. Reaction of PBr3 with a second ...
Chapter 25 & 26 Notes, part II
... Both alkenes and alkynes are considered unsaturated, because more hydrogens could be added if the double or triple bonds were broken. ...
... Both alkenes and alkynes are considered unsaturated, because more hydrogens could be added if the double or triple bonds were broken. ...
Mechanisms of organic reactions
... Again: initiation (creation of radicals), propagation (radicals attack neutral molecules, producing more and more radicals), termination (radicals react with each other, forming a stable product; the chain reaction is terminated) E.g.: polymerization of ethylene using dibenzoyl peroxide as an initia ...
... Again: initiation (creation of radicals), propagation (radicals attack neutral molecules, producing more and more radicals), termination (radicals react with each other, forming a stable product; the chain reaction is terminated) E.g.: polymerization of ethylene using dibenzoyl peroxide as an initia ...
CH 21 Organic Compounds I. Simple Organic Compounds A. All
... hex-6, hept-7, oct-8, non-9, dec-10 b) More carbons higher BP 2. Suffix tells type of bonding in molecule a) Saturated hydrocarbons have all single bondscalled alkanes 1) End with suffix ( –ane) ex) C2H6 is ethane 2) General formula: Cn H(2n + 2) a. ‘n’ stands for number of carbon atoms in formulas ...
... hex-6, hept-7, oct-8, non-9, dec-10 b) More carbons higher BP 2. Suffix tells type of bonding in molecule a) Saturated hydrocarbons have all single bondscalled alkanes 1) End with suffix ( –ane) ex) C2H6 is ethane 2) General formula: Cn H(2n + 2) a. ‘n’ stands for number of carbon atoms in formulas ...
Nucleophilic Substitution Reaction
... Elimination Reactions Elimination reactions, in which two groups are removed from a molecule, not being replaced by another group, are the reverse of addition reactions. Usually they involve the loss of two substituents from vicinal atoms resulting in the formation of a double or triple bond. Most c ...
... Elimination Reactions Elimination reactions, in which two groups are removed from a molecule, not being replaced by another group, are the reverse of addition reactions. Usually they involve the loss of two substituents from vicinal atoms resulting in the formation of a double or triple bond. Most c ...
Alkene reaction study guide
... o Look for differences between the original and the final compounds (for example, if there is a chlorine present at the beginning and none at the end, there must have been a dehydrohalogenation or epoxide formation from halohydrin). o If the starting compound is an alkane with no functional groups, ...
... o Look for differences between the original and the final compounds (for example, if there is a chlorine present at the beginning and none at the end, there must have been a dehydrohalogenation or epoxide formation from halohydrin). o If the starting compound is an alkane with no functional groups, ...
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.