organic chemistry
... • Naming: carbon prefix + -ene – A number is used in front to indicate the location of the double bond – If a number is not indicated the double bond comes after the 1st carbon ...
... • Naming: carbon prefix + -ene – A number is used in front to indicate the location of the double bond – If a number is not indicated the double bond comes after the 1st carbon ...
102 Lecture Ch11
... - can bond with other carbons to form chains and rings - can bond with a variety of other elements • Learning organic chemistry will help you understand the nature of the world around you: - pharmaceuticals, household products, plastics, etc. - essential for understanding biology and biochemistry ...
... - can bond with other carbons to form chains and rings - can bond with a variety of other elements • Learning organic chemistry will help you understand the nature of the world around you: - pharmaceuticals, household products, plastics, etc. - essential for understanding biology and biochemistry ...
Chapter 4 Summary
... The carbon skeletons of organic molecules vary in length and shape and have bonding sites for atoms of other elements. ...
... The carbon skeletons of organic molecules vary in length and shape and have bonding sites for atoms of other elements. ...
11.1 Organic Chemistry
... Cis-Trans Isomers • In alkenes with groups other than hydrogen, two different molecules are possible with the same formulas. Trans isomers have the groups diagonally opposite while cis isomers have the groups on the same side of a molecular axis. ...
... Cis-Trans Isomers • In alkenes with groups other than hydrogen, two different molecules are possible with the same formulas. Trans isomers have the groups diagonally opposite while cis isomers have the groups on the same side of a molecular axis. ...
gorgpps.pps - Knockhardy
... Individual students may use the material at home for revision purposes and it can also prove useful for classroom teaching with an interactive white board. Accompanying notes on this, and the full range of AS and A2 Chemistry topics, are available from the KNOCKHARDY WEBSITE at... ...
... Individual students may use the material at home for revision purposes and it can also prove useful for classroom teaching with an interactive white board. Accompanying notes on this, and the full range of AS and A2 Chemistry topics, are available from the KNOCKHARDY WEBSITE at... ...
Carbon and the Molecular Diversity of Life
... Carbon has four valence electrons. To complete its valence shell, carbon forms four covalent bonds with other atoms. The tetravalence of carbon is at the center of carbon’s ability to form large and complex molecules with characteristic three-dimensional shapes and properties. ...
... Carbon has four valence electrons. To complete its valence shell, carbon forms four covalent bonds with other atoms. The tetravalence of carbon is at the center of carbon’s ability to form large and complex molecules with characteristic three-dimensional shapes and properties. ...
8.2-Organic Nomenclature packet
... between the carbon atoms is shorter in the double bond. It is also more reactive than a single bond since the bond (the second pair of electrons) is farther from the nuclei. Naming is a little bit more complex for alkenes than alkanes. Since the double bond could appear at various sites in a typic ...
... between the carbon atoms is shorter in the double bond. It is also more reactive than a single bond since the bond (the second pair of electrons) is farther from the nuclei. Naming is a little bit more complex for alkenes than alkanes. Since the double bond could appear at various sites in a typic ...
Organic_Nomenclature_packet
... and the bond length between the carbon atoms is shorter in the double bond. It is also more reactive than a single bond since the bond (the second pair of electrons) is farther from the nuclei. Naming is a little bit more complex for alkenes than alkanes. Since the double bond could appear at vari ...
... and the bond length between the carbon atoms is shorter in the double bond. It is also more reactive than a single bond since the bond (the second pair of electrons) is farther from the nuclei. Naming is a little bit more complex for alkenes than alkanes. Since the double bond could appear at vari ...
Organic Nomenclature - Alkanes, Alkenes, Alkynes
... double bond. It is also more reactive than a single bond since the bond (the second pair of electrons) is farther from the nuclei. Naming is a little bit more complex for alkenes than alkanes. Since the double bond could appear at various sites in a typical molecule, we have to specify where it is ...
... double bond. It is also more reactive than a single bond since the bond (the second pair of electrons) is farther from the nuclei. Naming is a little bit more complex for alkenes than alkanes. Since the double bond could appear at various sites in a typical molecule, we have to specify where it is ...
Introduction to Organic Chemistry
... • An ether is a molecule consisting of two alkyl groups connected to an oxygen atom. • Ethers are named by considering one alkyl group (the shorter one) plus the oxygen atom to be a substituent and the other alkyl group (the longer one) to be an alkane. • The alkyl group plus oxygen atom is called a ...
... • An ether is a molecule consisting of two alkyl groups connected to an oxygen atom. • Ethers are named by considering one alkyl group (the shorter one) plus the oxygen atom to be a substituent and the other alkyl group (the longer one) to be an alkane. • The alkyl group plus oxygen atom is called a ...
Organic Chemistry Notes
... You will name and draw structural, condensed structural and line diagrams and formulas, using International Union of Pure and Applied Chemistry (IUPAC) nomenclature guidelines, for saturated and unsaturated aliphatic (including cyclic) and aromatic carbon compounds containing only one type of a func ...
... You will name and draw structural, condensed structural and line diagrams and formulas, using International Union of Pure and Applied Chemistry (IUPAC) nomenclature guidelines, for saturated and unsaturated aliphatic (including cyclic) and aromatic carbon compounds containing only one type of a func ...
Organic Compounds
... • Identify substances which contain organic compounds • Sketch and describe isomer structures ...
... • Identify substances which contain organic compounds • Sketch and describe isomer structures ...
Chapter 13 - WebAssign
... What is the difference between saturated and unsaturated hydrocarbons? Alkanes contain only single bonds and are saturated hydrocarbons because they cannot react with hydrogen to produce more C-H bonds. However, multiple (double or triple) bonds are unsaturated because an H2 molecule can add across ...
... What is the difference between saturated and unsaturated hydrocarbons? Alkanes contain only single bonds and are saturated hydrocarbons because they cannot react with hydrogen to produce more C-H bonds. However, multiple (double or triple) bonds are unsaturated because an H2 molecule can add across ...
organic chemistry - Mr. Walsh`s AP Chemistry
... - hydrocarbons are classified according to whether or not they have multiple bonds 1. Alkanes suffix -ane All bonds in carbon chain or ring are single bonds 2. Alkenes suffix -ene Hydrocarbon has one or more double bonds between carbon atoms 3. Alkynes suffix -yne Hydrocarbon has one or more triple ...
... - hydrocarbons are classified according to whether or not they have multiple bonds 1. Alkanes suffix -ane All bonds in carbon chain or ring are single bonds 2. Alkenes suffix -ene Hydrocarbon has one or more double bonds between carbon atoms 3. Alkynes suffix -yne Hydrocarbon has one or more triple ...
Carboxylic Acids
... B) Incomplete combustion - produce carbon , carbon monoxide, CO2 , H2O C2H6 + O2 C2H6 + O2 ...
... B) Incomplete combustion - produce carbon , carbon monoxide, CO2 , H2O C2H6 + O2 C2H6 + O2 ...
condensed review notes
... Alkenes are hydrocarbons containing a double bond between carbons that makes them more reactive than alkanes Alkenes undergo addition reactions with hydrogen, halogens, hydrogen halides and water via electrophilic addition and adhere to Markovnikov’s Rule. (*Tertiary carbocations intermediates a ...
... Alkenes are hydrocarbons containing a double bond between carbons that makes them more reactive than alkanes Alkenes undergo addition reactions with hydrogen, halogens, hydrogen halides and water via electrophilic addition and adhere to Markovnikov’s Rule. (*Tertiary carbocations intermediates a ...
chapter 12_LO - Faculty Websites
... What do the wedges represent in structural formulas? The dashed lines? What is the difference between chemical formulas, expanded structural formulas, condensed structural formulas, and line drawings? You should be able to easily convert between these different representations of organic compounds. ...
... What do the wedges represent in structural formulas? The dashed lines? What is the difference between chemical formulas, expanded structural formulas, condensed structural formulas, and line drawings? You should be able to easily convert between these different representations of organic compounds. ...
Organic Reactions
... • Reactions occur between electrophiles and nucleophiles. • Just about any part of a molecule can be either electrophilic or nucleophilic depending one what you are comparing it to ...
... • Reactions occur between electrophiles and nucleophiles. • Just about any part of a molecule can be either electrophilic or nucleophilic depending one what you are comparing it to ...
Organic Chemistry
... • Naming: carbon prefix + -ene – A number is used in front to indicate the location of the double bond – If a number is not indicated the double bond comes after the 1st carbon ...
... • Naming: carbon prefix + -ene – A number is used in front to indicate the location of the double bond – If a number is not indicated the double bond comes after the 1st carbon ...
OrganicChemistrySV
... Notice: There is no alkyne corresponding to the methane of the alkane series. That is b/c there must be at least 2 carbon atoms to form a triple bond. ...
... Notice: There is no alkyne corresponding to the methane of the alkane series. That is b/c there must be at least 2 carbon atoms to form a triple bond. ...
Alkane
In organic chemistry, an alkane, or paraffin (a historical name that also has other meanings), is a saturated hydrocarbon. Alkanes consist only of hydrogen and carbon atoms and all bonds are single bonds. Alkanes (technically, always acyclic or open-chain compounds) have the general chemical formula CnH2n+2. For example, Methane is CH4, in which n=1 (n being the number of Carbon atoms). Alkanes belong to a homologous series of organic compounds in which the members differ by a molecular mass of 14.03u (mass of a methanediyl group, —CH2—, one carbon atom of mass 12.01u, and two hydrogen atoms of mass ≈1.01u each). There are two main commercial sources: petroleum (crude oil) and natural gas.Each carbon atom has 4 bonds (either C-H or C-C bonds), and each hydrogen atom is joined to a carbon atom (H-C bonds). A series of linked carbon atoms is known as the carbon skeleton or carbon backbone. The number of carbon atoms is used to define the size of the alkane e.g., C2-alkane.An alkyl group, generally abbreviated with the symbol R, is a functional group or side-chain that, like an alkane, consists solely of single-bonded carbon and hydrogen atoms, for example a methyl or ethyl group.The simplest possible alkane (the parent molecule) is methane, CH4. There is no limit to the number of carbon atoms that can be linked together, the only limitation being that the molecule is acyclic, is saturated, and is a hydrocarbon. Waxes include examples of larger alkanes where the number of carbons in the carbon backbone is greater than about 17, above which the compounds are solids at standard ambient temperature and pressure (SATP).Alkanes are not very reactive and have little biological activity. All alkanes are colourless and odourless. Alkanes can be viewed as a molecular tree upon which can be hung the more biologically active/reactive portions (functional groups) of the molecule.