1 up to alkynes (4 days)
... Carbon is the element necessary to classify a compound as organic . . . One reason that carbon has its own branch of chemistry is that there are over 10 million known carbon compounds, and about 90% of new compounds synthesized each year contain carbon. ...
... Carbon is the element necessary to classify a compound as organic . . . One reason that carbon has its own branch of chemistry is that there are over 10 million known carbon compounds, and about 90% of new compounds synthesized each year contain carbon. ...
File - Loreto Science
... formed can react with the water to form the carboxylic acid and alcohol • This reverse reaction is called Hydrolysis • Hydrolysis will happen very easily in the presence of a base such as NaOH ...
... formed can react with the water to form the carboxylic acid and alcohol • This reverse reaction is called Hydrolysis • Hydrolysis will happen very easily in the presence of a base such as NaOH ...
Organic Chemistry PowerPoint
... Differ only in the geometry of their substituents. Alkenes are fairly structured due to their double bonds. Therefore, there are two arrangements of the substituents, cis and trans, that are noted in naming. Cis configurations- place the substituents on the same side of the double bond Trans configu ...
... Differ only in the geometry of their substituents. Alkenes are fairly structured due to their double bonds. Therefore, there are two arrangements of the substituents, cis and trans, that are noted in naming. Cis configurations- place the substituents on the same side of the double bond Trans configu ...
2. Organic Families Activity
... the line-bond formula of the compound. If more than one family is represented you must list all of them. Most organic compounds contain a structural characteristic of the alkane family. However, we do not classify a compound as an alkane unless this is the only family it belongs to. Example: ...
... the line-bond formula of the compound. If more than one family is represented you must list all of them. Most organic compounds contain a structural characteristic of the alkane family. However, we do not classify a compound as an alkane unless this is the only family it belongs to. Example: ...
OCR_Organic_Chemistry_AS_summary
... • Margarine is made by hydrogenating C=C double bonds in animal or vegetable fats and oils. Temperatures of only 60°C are needed. • Vegetable oils often contain high proportions of polyunsaturated and mono-unsaturated fats, and as a result are oils at room temperature. That makes them messy to sprea ...
... • Margarine is made by hydrogenating C=C double bonds in animal or vegetable fats and oils. Temperatures of only 60°C are needed. • Vegetable oils often contain high proportions of polyunsaturated and mono-unsaturated fats, and as a result are oils at room temperature. That makes them messy to sprea ...
Alkane Alkyl groups are represented by the R
... oxidation. Tertiary alcohols can be shown in text as: R3COH ...
... oxidation. Tertiary alcohols can be shown in text as: R3COH ...
Chapter 4-Carbon & Diversity of Life
... Consists of a carbon atom bonded to three hydrogen atoms Can be bonded to the carbon or a different atom Referred to as Methylated Compounds Addition of a methyl group to DNA effects gene expression and arrangement of methyl groups in sex hormones affects their shape and funtion Ex: 5-Methyl cytidin ...
... Consists of a carbon atom bonded to three hydrogen atoms Can be bonded to the carbon or a different atom Referred to as Methylated Compounds Addition of a methyl group to DNA effects gene expression and arrangement of methyl groups in sex hormones affects their shape and funtion Ex: 5-Methyl cytidin ...
File - mrs. whalen`s classes!
... alkane. Name it by replacing –yl with –oxy. Give it a position number. 3. Put it together! Amines Contains the functional group –NH2, -NHR or –NRR’ **Note that “R” refers to any alkyl group. R’ simply means a second alkyl group. Like alcohols, amines can be primary, secondary or tertiary, but the me ...
... alkane. Name it by replacing –yl with –oxy. Give it a position number. 3. Put it together! Amines Contains the functional group –NH2, -NHR or –NRR’ **Note that “R” refers to any alkyl group. R’ simply means a second alkyl group. Like alcohols, amines can be primary, secondary or tertiary, but the me ...
Organic Chemistry Powerpoint
... The diversity of organic compounds results from the uniqueness of carbon’s structure and bonding. Carbon atoms are unique in their ability to form long chains and rings of covalently bonded atoms. ...
... The diversity of organic compounds results from the uniqueness of carbon’s structure and bonding. Carbon atoms are unique in their ability to form long chains and rings of covalently bonded atoms. ...
Chemistry Final Test
... rxn. d, respectively. One of these reaction is first-order, and the other is second-order. The following data were collected for these two reactions: ...
... rxn. d, respectively. One of these reaction is first-order, and the other is second-order. The following data were collected for these two reactions: ...
Chapter 13 - WebAssign
... to produce more C-H bonds. However, multiple (double or triple) bonds are unsaturated because an H2 molecule can add across a multiple bond to form two C-H bonds. For example, ethene can be hydrogenated to ethane: H2C=CH2 + H2 → H3C-CH3. Thus, alkenes are unsaturated. Molecules with many double bond ...
... to produce more C-H bonds. However, multiple (double or triple) bonds are unsaturated because an H2 molecule can add across a multiple bond to form two C-H bonds. For example, ethene can be hydrogenated to ethane: H2C=CH2 + H2 → H3C-CH3. Thus, alkenes are unsaturated. Molecules with many double bond ...
File
... Producing Ethene by Cracking Ethane • Over time, high-temperature cracking of ethane, as illustrated below, became the preferred technological process. As you can see, molecules of hydrogen are “eliminated” from the ethane. ...
... Producing Ethene by Cracking Ethane • Over time, high-temperature cracking of ethane, as illustrated below, became the preferred technological process. As you can see, molecules of hydrogen are “eliminated” from the ethane. ...
CHE 312 Answers in BOLD RED EXAM 1 KEY (Ch. 16
... What reagent or sequence of reagents will convert butanoic acid into butanal (CH3CH2CH2CHO) A. H2 + Lindlar catalyst B. B2H6 ; then PCC in CH2Cl2 C. LiAlH4 ; H3O+ ; PCC in CH2Cl2 D. Na in NH3(l) ...
... What reagent or sequence of reagents will convert butanoic acid into butanal (CH3CH2CH2CHO) A. H2 + Lindlar catalyst B. B2H6 ; then PCC in CH2Cl2 C. LiAlH4 ; H3O+ ; PCC in CH2Cl2 D. Na in NH3(l) ...
Notes-C12-121
... Rules for Naming Branched-Chain Alkanes • Rule 1: Identify the longest continuous carbon chain and name that chain as the parent • Rule 2: Number the carbon atoms in the parent chain in such a way so that to give the lowest possible number for a substituent (alkyl group). • Rule 3: If only one subs ...
... Rules for Naming Branched-Chain Alkanes • Rule 1: Identify the longest continuous carbon chain and name that chain as the parent • Rule 2: Number the carbon atoms in the parent chain in such a way so that to give the lowest possible number for a substituent (alkyl group). • Rule 3: If only one subs ...
Science 30 Chemistry
... Alcohols and carboxylic acids react to form esters An H is removed from the alcohol and an ‘OH’ from the acid- water is formed. Functional group for ester: Naming an ester: R’ is the alcohol, change the ending to ‘yl’ R is the acid – drop ‘ic acid’ and change ending to ‘ate’ ...
... Alcohols and carboxylic acids react to form esters An H is removed from the alcohol and an ‘OH’ from the acid- water is formed. Functional group for ester: Naming an ester: R’ is the alcohol, change the ending to ‘yl’ R is the acid – drop ‘ic acid’ and change ending to ‘ate’ ...
condensed review notes
... Alkanes are generally unreactive, because both the C-C and C-H bonds are strong and also non-polar Alkanes have very similar electronegativities Alkanes undergo combustion – they burn very exothermically in oxygen to produce carbon dioxide CO2 and water H2O (this is complete combustion), for e ...
... Alkanes are generally unreactive, because both the C-C and C-H bonds are strong and also non-polar Alkanes have very similar electronegativities Alkanes undergo combustion – they burn very exothermically in oxygen to produce carbon dioxide CO2 and water H2O (this is complete combustion), for e ...
Elimination Reactions
... Explain how additions of water to an alkene and elimination of an alcohol are opposite mechanisms Describe how to shift equilibrium in favor of elimination or addition Predict the major product according to alkene stability Daily Problems 1. Provide a mechanism for these elimination reactions ...
... Explain how additions of water to an alkene and elimination of an alcohol are opposite mechanisms Describe how to shift equilibrium in favor of elimination or addition Predict the major product according to alkene stability Daily Problems 1. Provide a mechanism for these elimination reactions ...
Chapter 1: Chemistry and You
... 2014-2015 HONORS Chemistry Midterm Review This review sheet is a list of topics and sample practice problems only. The practice problems are good representation of what to expect on the midterm, but it is not enough to just study from the review. You need to look over your notes, old review sheets, ...
... 2014-2015 HONORS Chemistry Midterm Review This review sheet is a list of topics and sample practice problems only. The practice problems are good representation of what to expect on the midterm, but it is not enough to just study from the review. You need to look over your notes, old review sheets, ...
COVALENT BOND bond formed by the sharing of electrons
... Two atoms share one or more pairs of outer-shell ...
... Two atoms share one or more pairs of outer-shell ...
Phenomenologica lSignificanceof non identifical sp3
... investigations. In the case sp3-hybridization model of electron configuration of carbon atom is the key position of organic, organometallic, elementorganic chemistry, at identity of witch to nature of interaction have no doubt because of its simplicity and attractively. But investigations of the che ...
... investigations. In the case sp3-hybridization model of electron configuration of carbon atom is the key position of organic, organometallic, elementorganic chemistry, at identity of witch to nature of interaction have no doubt because of its simplicity and attractively. But investigations of the che ...
2008 Periodic Table of the Elements Instructions: Read carefully all
... Which of the following statements is NOT true concerning organic chemistry? a) Some organic compounds can be made from inorganic compounds. b) Organic chemistry is the chemistry of chemicals originating from living organisms. c) Organic chemistry is the chemistry of carbon-containing compounds. d) O ...
... Which of the following statements is NOT true concerning organic chemistry? a) Some organic compounds can be made from inorganic compounds. b) Organic chemistry is the chemistry of chemicals originating from living organisms. c) Organic chemistry is the chemistry of carbon-containing compounds. d) O ...
Practice Test 11 - U of L Class Index
... A chunk of white phosphorus weighing 6.58 grams is put in a 750 mL flask containing dry argon (which is then removed using a vacuum, leaving only the phosphorus in the flask). A separate 750 mL flask contains 3.15 bar of fluorine gas (at 19.65 °C). The two flasks are connected so that the two compou ...
... A chunk of white phosphorus weighing 6.58 grams is put in a 750 mL flask containing dry argon (which is then removed using a vacuum, leaving only the phosphorus in the flask). A separate 750 mL flask contains 3.15 bar of fluorine gas (at 19.65 °C). The two flasks are connected so that the two compou ...
Glossary of Key Terms in Chapter Two
... constitutional isomers (10.2) two molecules having the same molecular formulas but different chemical structures. cycloalkane (10.3) cyclic alkanes; saturated hydrocarbons, that have the general formula CnH2n. equatorial atom (10.4) an atom that lies in the plane of a cycloalkane ring. functional gr ...
... constitutional isomers (10.2) two molecules having the same molecular formulas but different chemical structures. cycloalkane (10.3) cyclic alkanes; saturated hydrocarbons, that have the general formula CnH2n. equatorial atom (10.4) an atom that lies in the plane of a cycloalkane ring. functional gr ...
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.