10.4b Organic Practice Test Version 2
... 3. Which one of the following statements best describes an elimination reaction? a) Carbon atoms in the organic product are bonded to fewer atoms than the carbon atoms in the organic reactant. b) A hydrogen atom or functional group is replaced with a different atom or functional group. c) Atoms are ...
... 3. Which one of the following statements best describes an elimination reaction? a) Carbon atoms in the organic product are bonded to fewer atoms than the carbon atoms in the organic reactant. b) A hydrogen atom or functional group is replaced with a different atom or functional group. c) Atoms are ...
Lesmahagow High School CfE Advanced Higher Chemistry Unit 2
... Boiling Points—most organic molecules contain mainly hydrogen and carbon. As the hydrocarbon chain increases in these molecules the strength of London dispersion forces also increases giving rise to a higher boiling point. As a result more energy is require to move the molecules further apart. Branc ...
... Boiling Points—most organic molecules contain mainly hydrogen and carbon. As the hydrocarbon chain increases in these molecules the strength of London dispersion forces also increases giving rise to a higher boiling point. As a result more energy is require to move the molecules further apart. Branc ...
Introduction to Organic Chemistry (aka carbon chemistry)
... The PROPERTIES OF ORGANIC COMPOUNDS are generally determined by three factors: a) The carbon skeleton is a very stable, chemically unreactive structure. b) The presence of double or triple bonds increases the reactivity of carbon skeletons. c) “Functional groups" which are reactive radicals attached ...
... The PROPERTIES OF ORGANIC COMPOUNDS are generally determined by three factors: a) The carbon skeleton is a very stable, chemically unreactive structure. b) The presence of double or triple bonds increases the reactivity of carbon skeletons. c) “Functional groups" which are reactive radicals attached ...
Reactions of Oxacyclopropanes
... 9-10 Sulfur Analogs of Alcohols and Ethers The sulfur analogs of alcohols and ethers are thiols and sulfides. The IUPAC system calls the sulfur analogs of alcohols, R-SH, “thiols.” The –SH group in more complicated compounds is referred to as “mercapto.” ...
... 9-10 Sulfur Analogs of Alcohols and Ethers The sulfur analogs of alcohols and ethers are thiols and sulfides. The IUPAC system calls the sulfur analogs of alcohols, R-SH, “thiols.” The –SH group in more complicated compounds is referred to as “mercapto.” ...
World of Carbon Flashcards
... the corresponding alkanes by changing one of the middle chain carbon atoms into a carbonyl group. ...
... the corresponding alkanes by changing one of the middle chain carbon atoms into a carbonyl group. ...
Hydrocarbon Derivatives
... –oic acid to –oate and is the main chain (name last) The name of the alkyl group from the alcohol ends in –yl ...
... –oic acid to –oate and is the main chain (name last) The name of the alkyl group from the alcohol ends in –yl ...
EX. Draw the structure of
... Naming and Drawing Alkyl Halides: Identify the root Identify the prefix: Name and number any alkyl side groups. Insert the number(s) of the carbon atom(s) bonded to the halogen(s). Use the prefix(es) that identify the specific halogen(s) ...
... Naming and Drawing Alkyl Halides: Identify the root Identify the prefix: Name and number any alkyl side groups. Insert the number(s) of the carbon atom(s) bonded to the halogen(s). Use the prefix(es) that identify the specific halogen(s) ...
Chapter 20 - Simpson County Schools
... Naming: Carbon atoms are numbered starting at one of the substituted groups. Numbering may be either clockwise or counterclockwise but must be done in the direction that gives the lowest possible numbers to the substituent groups. When the compound is named as a derivative of one of the special pa ...
... Naming: Carbon atoms are numbered starting at one of the substituted groups. Numbering may be either clockwise or counterclockwise but must be done in the direction that gives the lowest possible numbers to the substituent groups. When the compound is named as a derivative of one of the special pa ...
投影片 1
... a positive charge, whereas the other E class group resides on a carbon with a negative charge. ...
... a positive charge, whereas the other E class group resides on a carbon with a negative charge. ...
Taylor`s Organic Reactions Summary Sheet
... reactants, and must be considered in designing the synthesis of specific alkyl halides. These alkyl halides can then be transformed into other organic compounds. Preparing Organic Halides: Halogenation ...
... reactants, and must be considered in designing the synthesis of specific alkyl halides. These alkyl halides can then be transformed into other organic compounds. Preparing Organic Halides: Halogenation ...
Name
... b. C=O- carbonyl c. COOH- carboxyl d. NH2- amino e. OPO32-- phosphate f. CH3- methyl 5. What is the difference between a saturated and an unsaturated fatty acid? (1) Saturated fats do not have double bonded C and have the max number of H possible. Unsaturated have double bonds and not the max number ...
... b. C=O- carbonyl c. COOH- carboxyl d. NH2- amino e. OPO32-- phosphate f. CH3- methyl 5. What is the difference between a saturated and an unsaturated fatty acid? (1) Saturated fats do not have double bonded C and have the max number of H possible. Unsaturated have double bonds and not the max number ...
CHEM 201 Name Quiz 10 (Ch 17) ID Q1. Which of the following
... the ester shown below with LiAlH4? O O ...
... the ester shown below with LiAlH4? O O ...
Pre Ch15 HW
... For KEY TERMS: Make sure you can define it and/or give an example of it. Pick TWO terms of your choice and actually write the definition or an example. For KEY EQUATIONS AND RELATIONSHIP: Next to EACH, define each term. Be very specific. CHAPTER REVIEW GUIDE Learning Objectives Relevant section (§) ...
... For KEY TERMS: Make sure you can define it and/or give an example of it. Pick TWO terms of your choice and actually write the definition or an example. For KEY EQUATIONS AND RELATIONSHIP: Next to EACH, define each term. Be very specific. CHAPTER REVIEW GUIDE Learning Objectives Relevant section (§) ...
Unit 10 - Renton School District
... Compounds up to six carbon atoms (in the basic chain for nomenclature purposes) containing only one of the classes of functional groups: alcohols, ethers, aldehydes, halogenoalkanes, ketones, esters and carboxylic acids. ...
... Compounds up to six carbon atoms (in the basic chain for nomenclature purposes) containing only one of the classes of functional groups: alcohols, ethers, aldehydes, halogenoalkanes, ketones, esters and carboxylic acids. ...
Functional Groups and Preparations
... It was traditionally used as a solvent but was found to be carcinogenic so methyl benzene (toluene is now used instead) Would you predict it would be soluble in water or ...
... It was traditionally used as a solvent but was found to be carcinogenic so methyl benzene (toluene is now used instead) Would you predict it would be soluble in water or ...
ch02-chemistry
... 3. _______ A weak attraction between a slightly positive hydrogen atom in one molecule and a slightly negative oxygen or nitrogen atom in another 4. _______ The attraction of a cation to an anion ...
... 3. _______ A weak attraction between a slightly positive hydrogen atom in one molecule and a slightly negative oxygen or nitrogen atom in another 4. _______ The attraction of a cation to an anion ...
Reaction of Alkenes
... Alkyl halide (R‐X): A compound containing a halogen atom covalently bonded to an sp3‐carbon atom ...
... Alkyl halide (R‐X): A compound containing a halogen atom covalently bonded to an sp3‐carbon atom ...
Document
... Diazomethane forms methylene, which converts alkenes into cyclopropanes. The highly reactive species methylene, H2C: (the simplest carbene) can be produced from the decomposition of diazomethane: ...
... Diazomethane forms methylene, which converts alkenes into cyclopropanes. The highly reactive species methylene, H2C: (the simplest carbene) can be produced from the decomposition of diazomethane: ...
無投影片標題
... Solubility Although C — X bond is polar, it is not polar enough to have a significant effect on the solubility of haloalkanes and ...
... Solubility Although C — X bond is polar, it is not polar enough to have a significant effect on the solubility of haloalkanes and ...
File - TGHS Level 3 Chemistry
... acids (long chain acids). These salts are soluble in water as they are ionised, but they have a carbon chain end that is soluble in fats and oils. This allows them to dissolve and break down dirt. Sodium laurate is the name of the soap molecule made from coconut oil made by boiling it with sodium hy ...
... acids (long chain acids). These salts are soluble in water as they are ionised, but they have a carbon chain end that is soluble in fats and oils. This allows them to dissolve and break down dirt. Sodium laurate is the name of the soap molecule made from coconut oil made by boiling it with sodium hy ...
Reactions of Hydrocarbons & their functional groups
... • Aromatics can only undergo substitution reactions ...
... • Aromatics can only undergo substitution reactions ...
Chemistry
... 2. Explain the difference between 10, 20 and 30 alkyl halides, with suitable examples. 3. Allyl halides are more reactive than alkyl halides. Why? 4. What are the reagents required prepare alkyl halide from the following (i) alcohol (ii) alkene (iv) alkanes 5. Explain the reactions used to convert b ...
... 2. Explain the difference between 10, 20 and 30 alkyl halides, with suitable examples. 3. Allyl halides are more reactive than alkyl halides. Why? 4. What are the reagents required prepare alkyl halide from the following (i) alcohol (ii) alkene (iv) alkanes 5. Explain the reactions used to convert b ...
Functional Groups: Centers of Reactivity
... Benzene, C6H6, and its derivatives are examples of the class of organic compounds called aromatic: ...
... Benzene, C6H6, and its derivatives are examples of the class of organic compounds called aromatic: ...
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.