Excercises 6-10
... acid chloride. What is the name of this mechanism? What is the molecularity of this reaction in the rate-‐determining step? Why is this reaction different from a comparable SN2 reactio ...
... acid chloride. What is the name of this mechanism? What is the molecularity of this reaction in the rate-‐determining step? Why is this reaction different from a comparable SN2 reactio ...
Pre-lab 2: Naming and Modeling Organic Compounds
... bonds, but with double and triple bonds no rotation is possible. This makes the structures of double and triple bonded compounds more rigid. When rotation around a single bond occurs, several conformations are possible. Since no rotation is possible around double and triple bonds, only one conformat ...
... bonds, but with double and triple bonds no rotation is possible. This makes the structures of double and triple bonded compounds more rigid. When rotation around a single bond occurs, several conformations are possible. Since no rotation is possible around double and triple bonds, only one conformat ...
Some comments and hints for the March 9 Biochemistry
... c. The reduction of fructose creates a new tetrahedral stereocenter. This can be examined best by looking at Fischer projections of the sugars. d. The first method will convert the alcohols to methyl ethers. The second will produce silyl ethers. 2. The leaving group in hydrolysis, the amine, is more ...
... c. The reduction of fructose creates a new tetrahedral stereocenter. This can be examined best by looking at Fischer projections of the sugars. d. The first method will convert the alcohols to methyl ethers. The second will produce silyl ethers. 2. The leaving group in hydrolysis, the amine, is more ...
Diol Oxidation Handout
... Diol Oxidation Puzzle Introduction: In this experiment, you will use household bleach, a mild oxidizing agent, to oxidize a diol containing compound. You may either use 2-ethyl-1,3-hexanediol or 2,2,4-trimethyl-1,3-pentanediol for your reaction. HO ...
... Diol Oxidation Puzzle Introduction: In this experiment, you will use household bleach, a mild oxidizing agent, to oxidize a diol containing compound. You may either use 2-ethyl-1,3-hexanediol or 2,2,4-trimethyl-1,3-pentanediol for your reaction. HO ...
This exam will consist of 30-35 multiple choice or short answer
... Briefly explain how structure of the alkyl halide substrate affects reactivity in SN2 and SN1 reactions. Why does 1-bromobutane react faster than 1-chlorobutane? Explain the two types of reactions used in this experiment to determine SN2 and SN1 reactivity. How could you tell a reaction was occurrin ...
... Briefly explain how structure of the alkyl halide substrate affects reactivity in SN2 and SN1 reactions. Why does 1-bromobutane react faster than 1-chlorobutane? Explain the two types of reactions used in this experiment to determine SN2 and SN1 reactivity. How could you tell a reaction was occurrin ...
File
... Amides and carboxylic acids both contain carbonyl groups. Amides have the carbonyl carbon bonded to a nitrogen atom, but carboxylic acids have the carbonyl carbon bonded to a hydroxyl group. 19. What happens to the double bond of a monomer participating in the formation of an addition polymer? One o ...
... Amides and carboxylic acids both contain carbonyl groups. Amides have the carbonyl carbon bonded to a nitrogen atom, but carboxylic acids have the carbonyl carbon bonded to a hydroxyl group. 19. What happens to the double bond of a monomer participating in the formation of an addition polymer? One o ...
MULTISTEP SYNTHESIS PROTECTING GROUPS
... Sulfonyl chlorides contain a good leaving group (Cl). That is what makes them highly reactive towards water and other nucleophiles such as ammonia (NH3). These reactions are used in this synthesis, but they can also cause problems. For example, the second step of the synthesis transforms p-acetamido ...
... Sulfonyl chlorides contain a good leaving group (Cl). That is what makes them highly reactive towards water and other nucleophiles such as ammonia (NH3). These reactions are used in this synthesis, but they can also cause problems. For example, the second step of the synthesis transforms p-acetamido ...
ANSWERS: Types of Reactions - Chemical Minds
... 6) Addition – occurs in alkenes because they have double bonds. Ethene is an alkene so will undergo addition reactions. The chlorine (molecule) will add (across the double bond.) CH2 = CH2 + Cl2 → CH2Cl – CH2Cl Substitution occurs in alkanes (because they have single bonds). Ethane is an alkane, so ...
... 6) Addition – occurs in alkenes because they have double bonds. Ethene is an alkene so will undergo addition reactions. The chlorine (molecule) will add (across the double bond.) CH2 = CH2 + Cl2 → CH2Cl – CH2Cl Substitution occurs in alkanes (because they have single bonds). Ethane is an alkane, so ...
Organic Lab
... compounds known, it has been helpful to chemists to divide these compounds into families, based on what functional group they contain. Generally it is found that all the members of a family containing a particular functional group will have many similar physical properties and will undergo similar c ...
... compounds known, it has been helpful to chemists to divide these compounds into families, based on what functional group they contain. Generally it is found that all the members of a family containing a particular functional group will have many similar physical properties and will undergo similar c ...
Chapter 17: Molecular Modeling Problems
... triphenylphosphine ylide. Which Lewis structure appears to be the more appropriate? Explain how you reached your conclusion. 8. Wittig Reaction. CO double bonds are typically much stronger that CC double bonds, making it difficult obtain alkenes from carbonyl compounds. The Wittig reaction offers a ...
... triphenylphosphine ylide. Which Lewis structure appears to be the more appropriate? Explain how you reached your conclusion. 8. Wittig Reaction. CO double bonds are typically much stronger that CC double bonds, making it difficult obtain alkenes from carbonyl compounds. The Wittig reaction offers a ...
File - Mr. Heff`s Class
... - Melting point = 5.5 oC, boiling point = 80.1 oC which is comparable to the boiling of cyclohexane (81.4 0C). - Non-polar molecule and is soluble only in nonpolar solvents. - Benzene has hybrid bonds. - Benzene is a planar molecule - Benzene molecules behave like alkanes in chemical reactions, not ...
... - Melting point = 5.5 oC, boiling point = 80.1 oC which is comparable to the boiling of cyclohexane (81.4 0C). - Non-polar molecule and is soluble only in nonpolar solvents. - Benzene has hybrid bonds. - Benzene is a planar molecule - Benzene molecules behave like alkanes in chemical reactions, not ...
File
... For example, propan-1-ol is produced by the hydroboration-oxidation reaction of propene. In this reaction, propene reacts with diborane (BH3)2 to form trialkyl borane as an addition product. This addition product is oxidized to alcohol by hydrogen peroxide in the presence of aqueous sodium hydroxide ...
... For example, propan-1-ol is produced by the hydroboration-oxidation reaction of propene. In this reaction, propene reacts with diborane (BH3)2 to form trialkyl borane as an addition product. This addition product is oxidized to alcohol by hydrogen peroxide in the presence of aqueous sodium hydroxide ...
Page 1 - WordPress.com
... Q5.Hexane (C6H14) is a member of the homologous series of alkanes. (a) (i) Name the raw material from which hexane is obtained. (1) (ii) Name the process used to ...
... Q5.Hexane (C6H14) is a member of the homologous series of alkanes. (a) (i) Name the raw material from which hexane is obtained. (1) (ii) Name the process used to ...
today`s PowerPoint
... • Both aldehydes and ketones will test positively. No other compounds (e.g. Carboxylic acids or esters) will • The precipitate is called 2,4-dinitrophenylhydrazone ...
... • Both aldehydes and ketones will test positively. No other compounds (e.g. Carboxylic acids or esters) will • The precipitate is called 2,4-dinitrophenylhydrazone ...
Document
... H bonding in polar compd. Stronger than alcohol because OH is more polarized (presence of e– carbonyl groups) ...
... H bonding in polar compd. Stronger than alcohol because OH is more polarized (presence of e– carbonyl groups) ...
Chapter 4 - Nomenclature and Conformations of Alkanes and
... - A plot of the melting points of unbranched alkane chains for the even sets separated from the odd sets will yield a smooth trend. However, when superimposed, it is clear that the even-numbered carbons have higher melting points than their nearby odd-number analogues - Branching that produces highl ...
... - A plot of the melting points of unbranched alkane chains for the even sets separated from the odd sets will yield a smooth trend. However, when superimposed, it is clear that the even-numbered carbons have higher melting points than their nearby odd-number analogues - Branching that produces highl ...
Chapter 24. Amines
... The hydrogens that can be eliminated are covalently attached to the carbon bound to the Nitrogen. In this case, there are 2 such places where a hydrogen could be eliminated to give the ...
... The hydrogens that can be eliminated are covalently attached to the carbon bound to the Nitrogen. In this case, there are 2 such places where a hydrogen could be eliminated to give the ...
ELECTROPHILIC ADDITIONS OF ALKENES AS THE
... Elimination results in net loss of HBr to form a new C=C bond. ...
... Elimination results in net loss of HBr to form a new C=C bond. ...
Ketones - WordPress.com
... orange precipitate with 2,4-DNPH. To differentiate, we may react the solution with Tollens’ reagent – a solution of silver nitrate in excess ...
... orange precipitate with 2,4-DNPH. To differentiate, we may react the solution with Tollens’ reagent – a solution of silver nitrate in excess ...
ABCT2423
... reactions: molecular structure, solvent, nucleophile, leaving group and neighbouring group. Alcohols, Phenols, Ethers and Thiols Structure, reactivity and preparation; hydrogen bonding; acidity; dehydration; oxidation. Aldehydes and Ketones Structure, properties and reactions; oxidation; nucleophili ...
... reactions: molecular structure, solvent, nucleophile, leaving group and neighbouring group. Alcohols, Phenols, Ethers and Thiols Structure, reactivity and preparation; hydrogen bonding; acidity; dehydration; oxidation. Aldehydes and Ketones Structure, properties and reactions; oxidation; nucleophili ...
General properties of urea : It is water
... General properties of urea : It is water-soluble crystalline compound acting only as a weak base giving sparingly soluble salts with HNO3 and ethanedioic acid (COOH)2 . In its chemical properties, urea gives the typical reaction expected from an amide (twice over) Its properties are essentially thos ...
... General properties of urea : It is water-soluble crystalline compound acting only as a weak base giving sparingly soluble salts with HNO3 and ethanedioic acid (COOH)2 . In its chemical properties, urea gives the typical reaction expected from an amide (twice over) Its properties are essentially thos ...
Chapter 3. The Concept of Protecting Functional Groups
... Since thioacetals are quite stable toward hydrolysis, there is no special need to remove the H2O formed during the reaction. Since it is more difficult to equilibrate thioacetals than acetal via protonation, double bond migration in thioacetalization of enones is not usually observed. ...
... Since thioacetals are quite stable toward hydrolysis, there is no special need to remove the H2O formed during the reaction. Since it is more difficult to equilibrate thioacetals than acetal via protonation, double bond migration in thioacetalization of enones is not usually observed. ...
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.