ADDITION REACTIONS
... the joining together of a large number of repeating units, called monomers, by a process of polymerisation. • Polymers,can be made artificially and these are usually referred to as plastics, but there are also a great number of naturally occurring polymers. • One type of polymerisation reaction is k ...
... the joining together of a large number of repeating units, called monomers, by a process of polymerisation. • Polymers,can be made artificially and these are usually referred to as plastics, but there are also a great number of naturally occurring polymers. • One type of polymerisation reaction is k ...
Study Guide for Exam 2 Chapter 12
... with more than one substituent on the benzene ring, and those in which the benzene ring is regarded as a substituent (phenyl ) group. From their names, draw structural formulas of aromatic compounds including types of compounds listed in the preceding item. Know the names and structures for the foll ...
... with more than one substituent on the benzene ring, and those in which the benzene ring is regarded as a substituent (phenyl ) group. From their names, draw structural formulas of aromatic compounds including types of compounds listed in the preceding item. Know the names and structures for the foll ...
Text questions - Corwin - Teach-n-Learn-Chem
... 19. The unsaturated hydrocarbons are the _________, which have one or more double bonds, and the ___________, which have one or more __________ bonds. 20. To name an alkene: A. Name the alkene for the longest continuous carbon chain that… B. Number the carbon chain starting from… The lowest number p ...
... 19. The unsaturated hydrocarbons are the _________, which have one or more double bonds, and the ___________, which have one or more __________ bonds. 20. To name an alkene: A. Name the alkene for the longest continuous carbon chain that… B. Number the carbon chain starting from… The lowest number p ...
Reactions of Hydrocarbons & their functional groups
... CH3-CH2-OH + HCl CH3-CH2Cl + H2O • The reverse reaction: CH3-CH2Cl + OHCH3-CH2-OH + Cl(from water) ...
... CH3-CH2-OH + HCl CH3-CH2Cl + H2O • The reverse reaction: CH3-CH2Cl + OHCH3-CH2-OH + Cl(from water) ...
handout alkenes from alcohols
... Elimination reactions. In this experiment, cyclohexanol will be dehydrated (loss of H2O) to form cyclohexene under acidic conditions (see Figure 1). ...
... Elimination reactions. In this experiment, cyclohexanol will be dehydrated (loss of H2O) to form cyclohexene under acidic conditions (see Figure 1). ...
handout alkenes from alcohols
... Elimination reactions. In this experiment, cyclohexanol will be dehydrated (loss of H2O) to form cyclohexene under acidic conditions (see Figure 1). ...
... Elimination reactions. In this experiment, cyclohexanol will be dehydrated (loss of H2O) to form cyclohexene under acidic conditions (see Figure 1). ...
Chemistry 0310 - Organic Chemistry 1 Chapter 12. Reactions of
... - Syn-Hydroxylations of alkenes are most conveniently performed with catalytic OsO4 and NMO (N-methylmorpholine N-oxide) as co-oxidant. Attack occurs from the less-hindered face of the alkene, and a vicinal syn-diol is isolated after reductive workup. - Oxidative cleavage of 1,2-disubstituted alken ...
... - Syn-Hydroxylations of alkenes are most conveniently performed with catalytic OsO4 and NMO (N-methylmorpholine N-oxide) as co-oxidant. Attack occurs from the less-hindered face of the alkene, and a vicinal syn-diol is isolated after reductive workup. - Oxidative cleavage of 1,2-disubstituted alken ...
ch08 by dr. Dina
... The initial syn addition of the oxygens is preserved when the oxygen-metal bonds are cleaved and the products are syn diols ...
... The initial syn addition of the oxygens is preserved when the oxygen-metal bonds are cleaved and the products are syn diols ...
Reaction of Alkenes
... alkenes, the electrophile adds to the least substituted carbon giving rise to the more stable intermediate. Example: Addition of HX Markovnikov Addition (only product) ...
... alkenes, the electrophile adds to the least substituted carbon giving rise to the more stable intermediate. Example: Addition of HX Markovnikov Addition (only product) ...
ALKENES and SULPHURIC ACID
... This is typical of the reaction with unsymmetrical alkenes. An unsymmetrical alkene has different groups at either end of the carbon-carbon double bond. If sulphuric acid adds to an unsymmetrical alkene like propene, there are two possible ways it could add. You could end up with one of two product ...
... This is typical of the reaction with unsymmetrical alkenes. An unsymmetrical alkene has different groups at either end of the carbon-carbon double bond. If sulphuric acid adds to an unsymmetrical alkene like propene, there are two possible ways it could add. You could end up with one of two product ...
Section D19: Alkanes, Alkenes and Alcohols
... and incomplete combustion of alkanes 3.5 describe the substitution reaction of methane with bromine to form bromomethane in the presence of UV light. 3.6 recall that alkenes have the general formula CnH2n 3.7 draw displayed formulae for alkenes with up to four carbon atoms in a molecule, and name th ...
... and incomplete combustion of alkanes 3.5 describe the substitution reaction of methane with bromine to form bromomethane in the presence of UV light. 3.6 recall that alkenes have the general formula CnH2n 3.7 draw displayed formulae for alkenes with up to four carbon atoms in a molecule, and name th ...
Alkenes: Overview
... •This double bond is the source of the reactivity of these molecules. •One of the major types of reactivity is ADDITION. •The colour of Br2 disappears! This can be used to detect the presence of a C - C double bond. ...
... •This double bond is the source of the reactivity of these molecules. •One of the major types of reactivity is ADDITION. •The colour of Br2 disappears! This can be used to detect the presence of a C - C double bond. ...
ORGANIC CHEMISTRY I – REVIEW FOR FINAL EXAM
... Industrial Preparation and Use of Alkenes Calculating a Molecule’s Degree of Unsaturation Naming Alkenes Electronic Structure of Alkenes Cis-Trans Isomerism in Alkenes Sequence Rules: The E,Z Designation Alkene Stability Electrophilic Addition of HX to Alkenes Orientation of Electrophilic Addition: ...
... Industrial Preparation and Use of Alkenes Calculating a Molecule’s Degree of Unsaturation Naming Alkenes Electronic Structure of Alkenes Cis-Trans Isomerism in Alkenes Sequence Rules: The E,Z Designation Alkene Stability Electrophilic Addition of HX to Alkenes Orientation of Electrophilic Addition: ...
Document
... Isomers have the same chemical formula (same amount of ‘stuff’) but a different structural formula (‘different layout’) For the first three members of the alkanes only one structure is possible but butane, C4H10, has two isomers; ...
... Isomers have the same chemical formula (same amount of ‘stuff’) but a different structural formula (‘different layout’) For the first three members of the alkanes only one structure is possible but butane, C4H10, has two isomers; ...
Double Bond
... Hydrogen gas and an alkene will react when mixed in the presence of a catalyst such as platinum or palladium. Two hydrogen atoms are added to the alkene in a reaction called hydrogenation, which is very exothermic. The heat released is called the “heat of hydrogenation” and has a typical value of ab ...
... Hydrogen gas and an alkene will react when mixed in the presence of a catalyst such as platinum or palladium. Two hydrogen atoms are added to the alkene in a reaction called hydrogenation, which is very exothermic. The heat released is called the “heat of hydrogenation” and has a typical value of ab ...
Alkene
In organic chemistry, an alkene is an unsaturated hydrocarbon that contains at least one carbon–carbon double bond. Alkene, olefin, and olefine are used often interchangeably (see nomenclature section below). Acyclic alkenes, with only one double bond and no other functional groups, known as mono-enes, form a homologous series of hydrocarbons with the general formula CnH2n. Alkenes have two hydrogen atoms less than the corresponding alkane (with the same number of carbon atoms). The simplest alkene, ethylene (C2H4), which has the International Union of Pure and Applied Chemistry (IUPAC) name ethene is the organic compound produced on the largest scale industrially. Aromatic compounds are often drawn as cyclic alkenes, but their structure and properties are different and they are not considered to be alkenes.