unit (7) organic compounds: hydrocarbons
... Alkanes are called saturated hydrocarbons because only single bonds connect carbons to each other and to other hydrogen atoms. The molecular formula of all alkanes fit the general formula CnH2n+2, where n equals the number of carbon atoms. There are several methods used to represent organic molecule ...
... Alkanes are called saturated hydrocarbons because only single bonds connect carbons to each other and to other hydrogen atoms. The molecular formula of all alkanes fit the general formula CnH2n+2, where n equals the number of carbon atoms. There are several methods used to represent organic molecule ...
Crown ethers
... These compounds are called Crown ethers because their molecule have a crown-like shape. The bracket number represents the ring size and the terminal numbers gives the number of oxygens. The oxygens are usually separated by two ...
... These compounds are called Crown ethers because their molecule have a crown-like shape. The bracket number represents the ring size and the terminal numbers gives the number of oxygens. The oxygens are usually separated by two ...
Lecture6-Organometallic Chemistry
... desired product with minimum amounts of side product. In industry there is considerable economic incentive to develop selective catalysts (b) Lifetime • A small amount of catalyst must survive through a large number of cycles of it is to be economically viable • A catalyst may be destroyed by side r ...
... desired product with minimum amounts of side product. In industry there is considerable economic incentive to develop selective catalysts (b) Lifetime • A small amount of catalyst must survive through a large number of cycles of it is to be economically viable • A catalyst may be destroyed by side r ...
Carbon, because of its valence electrons, can form four bonds and
... Although structural isomers have the same chemical formula, because the atoms are arranged differently, the compounds are named differently and have different properties. Geometric Isomers—isomers in which the order of atom bonding is the same but the arrangement of atoms in space is different. 2 Ty ...
... Although structural isomers have the same chemical formula, because the atoms are arranged differently, the compounds are named differently and have different properties. Geometric Isomers—isomers in which the order of atom bonding is the same but the arrangement of atoms in space is different. 2 Ty ...
2002
... (a) How do you account for the fact that aryl and alkenyl halides are less reactive towards nucleophilic substitution reactions? ...
... (a) How do you account for the fact that aryl and alkenyl halides are less reactive towards nucleophilic substitution reactions? ...
Substitution reactions of carbonyl compounds at the α
... 2b. Alkylation of Enolates Normal enolates formed by the action of LDA or NaH can generally be alkylated with alkyl iodides, bromides or tosylates, or benzylic or allylic halides. However, these reactions can sometimes be difficult to perform in high yield. A few methods do exist which allow enolate ...
... 2b. Alkylation of Enolates Normal enolates formed by the action of LDA or NaH can generally be alkylated with alkyl iodides, bromides or tosylates, or benzylic or allylic halides. However, these reactions can sometimes be difficult to perform in high yield. A few methods do exist which allow enolate ...
Solution 1. - TutorBreeze.com
... condense in the presence of aqueos sodium hydroxide to form aldol. ...
... condense in the presence of aqueos sodium hydroxide to form aldol. ...
Samantha Landolfa Amy Ryan Section 10 Experiment 9 – Alkenes
... elimination reaction. The rates of reactivity are tertiary > secondary > primary. An E1 reaction is favored when a tertiary alcohol is reacted in the presence of an acid. A carbocation intermediate forms and the products follow Zaitsev’s Rule, which states that the major product will be the most sub ...
... elimination reaction. The rates of reactivity are tertiary > secondary > primary. An E1 reaction is favored when a tertiary alcohol is reacted in the presence of an acid. A carbocation intermediate forms and the products follow Zaitsev’s Rule, which states that the major product will be the most sub ...
Learning Guide for Chapter 8
... we don't always worry about these Does the reaction stop at the product shown? What other products would be formed? nope - the product could react with another Cl radical CH2Cl, CHCl3, CCl4 Many radical reactions are also chain reactions. Is this one? How can you tell? yes! the radical needed to rea ...
... we don't always worry about these Does the reaction stop at the product shown? What other products would be formed? nope - the product could react with another Cl radical CH2Cl, CHCl3, CCl4 Many radical reactions are also chain reactions. Is this one? How can you tell? yes! the radical needed to rea ...
Chemistry Crunch #12.2: Organic Reactions KEY Why? Learning
... One hydrogen from the methane switches with one bromine. 3. Summarize. In a characteristic substitution reaction: a) There will always be 2 reactant(s) and 2 product(s). (give a #) (give a #) b) Describe a substitution reaction in general terms (meaning without referencing any specific elements or a ...
... One hydrogen from the methane switches with one bromine. 3. Summarize. In a characteristic substitution reaction: a) There will always be 2 reactant(s) and 2 product(s). (give a #) (give a #) b) Describe a substitution reaction in general terms (meaning without referencing any specific elements or a ...
Chapter 7 + 8
... Due to the 3-centered intermediate, dihalogen additions occur with an anti addition ...
... Due to the 3-centered intermediate, dihalogen additions occur with an anti addition ...
with answers
... two of these,, and draw their Lewis formulae, give their correct names, and state which class of organic compound each of them belongs to. (3P) ...
... two of these,, and draw their Lewis formulae, give their correct names, and state which class of organic compound each of them belongs to. (3P) ...
Topic 8 specification content - A
... I can describe the formation of major and minor products in addition reactions of unsymmetrical alkenes, and explain the formation of major and minor products by reference to the relative stabilities of primary, secondary and tertiary carbocation intermediates ...
... I can describe the formation of major and minor products in addition reactions of unsymmetrical alkenes, and explain the formation of major and minor products by reference to the relative stabilities of primary, secondary and tertiary carbocation intermediates ...
File - cpprashanths Chemistry
... (b)(i)CH3COCH3+[H]/Ni→CH3CH(OH)CH3+Con.H2SO4→CH3CH=CH2(1) (ii)C6H5COOH+SOCl2→C6H5COCl +H2 /PdBaSO4 →C6H5CHO (1) (iii)2CH3CH2OH +Mild oxidation (KMnO4 )→2CH3OH +NaOH→CH3CH3 (OH)CH2CHO (1) OR a) i) Aldol condensation; give the equation. ii) Acetone is treated with methyl magnesium bromide followed by ...
... (b)(i)CH3COCH3+[H]/Ni→CH3CH(OH)CH3+Con.H2SO4→CH3CH=CH2(1) (ii)C6H5COOH+SOCl2→C6H5COCl +H2 /PdBaSO4 →C6H5CHO (1) (iii)2CH3CH2OH +Mild oxidation (KMnO4 )→2CH3OH +NaOH→CH3CH3 (OH)CH2CHO (1) OR a) i) Aldol condensation; give the equation. ii) Acetone is treated with methyl magnesium bromide followed by ...
NUCLEOPHILIC SUBSTITUTION & ELIMINATION ON Csp 3
... - Haloalkanes can be converted to alcohols, thioalcohols, ethers, thioethers, amines, nitriles, azides, peroxides, . . . and a number of other type compounds - The predominant reaction types in these conversions are second order nulcleophilic substitutions, SN2 - SN2 reaction can be shown to depend ...
... - Haloalkanes can be converted to alcohols, thioalcohols, ethers, thioethers, amines, nitriles, azides, peroxides, . . . and a number of other type compounds - The predominant reaction types in these conversions are second order nulcleophilic substitutions, SN2 - SN2 reaction can be shown to depend ...
Hydrocarbons - msottchemistry
... are difficult to break. (This is why alkanes are relatively unreactive) • Can undergo combustion reactions and substitution reactions ...
... are difficult to break. (This is why alkanes are relatively unreactive) • Can undergo combustion reactions and substitution reactions ...
Substitution Reactions of Alcohols
... react an alcohol with an appropriate sulfonyl chloride in the presence of an amine ...
... react an alcohol with an appropriate sulfonyl chloride in the presence of an amine ...
Converting Alcohols to Alkyl Halides – The Mitsunobu Reaction
... react an alcohol with an appropriate sulfonyl chloride in the presence of an amine ...
... react an alcohol with an appropriate sulfonyl chloride in the presence of an amine ...
... mixtures are exposed to ultraviolet light. These are substitution reactions. Burn in air to form carbon dioxide, water and large amounts of energy. Undergo addition reactions with o Hydrogen to form alkanes o Halogens to form dihaloalkanes o Hydrogen halides to form haloalkanes o Water to form alkan ...
Word - chemmybear.com
... Know that “saturated” means “saturated with hydrogens” and describes alkanes. Know that alkenes, alkynes, and cyclic hydrocarbons are all “unsaturated.” State why unsaturated fats are better for you (the double bond makes them easier to digest and less likely to coat the inside of your arterie ...
... Know that “saturated” means “saturated with hydrogens” and describes alkanes. Know that alkenes, alkynes, and cyclic hydrocarbons are all “unsaturated.” State why unsaturated fats are better for you (the double bond makes them easier to digest and less likely to coat the inside of your arterie ...
Organic Chemistry Review
... Organic Chemistry Review • Organic compounds contain carbon atoms that are bonded to one another in chains, rings, and networks to form a variety of structures (polymers, oils, and other large molecules). • Carbon has four valence electrons and always makes four covalent bonds with other atoms. ...
... Organic Chemistry Review • Organic compounds contain carbon atoms that are bonded to one another in chains, rings, and networks to form a variety of structures (polymers, oils, and other large molecules). • Carbon has four valence electrons and always makes four covalent bonds with other atoms. ...
ORGANIC REACTIONS IN A CLAY MICROENVIRONMENT
... thio-ethers; (d) carboxylic acids, to give esters. The number of products obtained in each reaction depends on the ease of rearrangement of the carbocation intermediates. High yields are obtained where a single carbocation intermediate is formed, A variety of elimination reactions is also catalysed ...
... thio-ethers; (d) carboxylic acids, to give esters. The number of products obtained in each reaction depends on the ease of rearrangement of the carbocation intermediates. High yields are obtained where a single carbocation intermediate is formed, A variety of elimination reactions is also catalysed ...
SAMPLE QUESTION PAPER CHEMISTRY (043) CLASS XII (2013-14)
... a) Because due to high electro negativity of N, electron pair is more readily available in NH3 than in PH3 as electro negativity decreases on moving down the group ...
... a) Because due to high electro negativity of N, electron pair is more readily available in NH3 than in PH3 as electro negativity decreases on moving down the group ...
Alkenes - Calderglen High School
... Calderglen High Chemistry Nature’s Chemistry Alkenes Homework 13. The key below shows the name and general formula of some families of hydrocarbons. ...
... Calderglen High Chemistry Nature’s Chemistry Alkenes Homework 13. The key below shows the name and general formula of some families of hydrocarbons. ...
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.