Organic Chemistry The chemistry of carbon compounds. Carbon
... This test used to distinguish between alcohols according to rate of reaction 30> 20> 10> methanol Tertiary alcohol reacts directly with Lucas reagent. 3- Oxidation by cold KMnO4 KMnO4/ H2O ...
... This test used to distinguish between alcohols according to rate of reaction 30> 20> 10> methanol Tertiary alcohol reacts directly with Lucas reagent. 3- Oxidation by cold KMnO4 KMnO4/ H2O ...
Powerpoint File - University of Evansville Faculty Web sites
... make compounds containing these groups hydrophilic, and therefore soluble in water - a necessary condition for their roles in water-based life. Note that many biological molecules have two or more functional groups (e.g., amino acids - contain at least one carboxyl as well as one amino group). ...
... make compounds containing these groups hydrophilic, and therefore soluble in water - a necessary condition for their roles in water-based life. Note that many biological molecules have two or more functional groups (e.g., amino acids - contain at least one carboxyl as well as one amino group). ...
Organic Chemistry: Chemistry that involves Carbon
... carbon double bond C=C. They are also considered HYDROCARBONS. Alkenes are reactive hydrocarbons due to the presence of the C=C bonds which can be broken. They also burn in Oxygen to form Carbon dioxide, water and liberate energy. Task: Draw the structural formula for: Propene, butene and pentene. ...
... carbon double bond C=C. They are also considered HYDROCARBONS. Alkenes are reactive hydrocarbons due to the presence of the C=C bonds which can be broken. They also burn in Oxygen to form Carbon dioxide, water and liberate energy. Task: Draw the structural formula for: Propene, butene and pentene. ...
Document
... • Depending on the reagent, the two new OH groups can be added to the opposite sides (anti addition) or the same side (syn addition) of the double bond. ...
... • Depending on the reagent, the two new OH groups can be added to the opposite sides (anti addition) or the same side (syn addition) of the double bond. ...
Organic Chemistry
... This designates the parent chain and the root word of the molecule. • 2. Number the parent chain such that the branch (substituent) falls on the lowest carbon number. • 3. Count the number of carbons in the branched chain. Use the same set of root words EXCEPT add the suffix –yl. ...
... This designates the parent chain and the root word of the molecule. • 2. Number the parent chain such that the branch (substituent) falls on the lowest carbon number. • 3. Count the number of carbons in the branched chain. Use the same set of root words EXCEPT add the suffix –yl. ...
HW Ch#5 Alcohols - Seattle Central
... (a) Prednisone contains three ketones, one primary alcohol, one tertiary alcohol, one disubstituted carbon-carbon double bond, and one trisubstituted carboncarbon double bond. (b) Estradiol contains one secondary alcohol and one disubstituted phenol. ...
... (a) Prednisone contains three ketones, one primary alcohol, one tertiary alcohol, one disubstituted carbon-carbon double bond, and one trisubstituted carboncarbon double bond. (b) Estradiol contains one secondary alcohol and one disubstituted phenol. ...
Chapter 13 - WebAssign
... 27. Define polymer. Why is nylon 66 called a condensation polymer? 36. Identify each of the following pairs of molecules as constitutional 28. What is the difference between a polyamide and a polypeptide? ...
... 27. Define polymer. Why is nylon 66 called a condensation polymer? 36. Identify each of the following pairs of molecules as constitutional 28. What is the difference between a polyamide and a polypeptide? ...
Lesson Plan
... Nuffield Advanced Chemistry students book (I used fourth edition) is good, it has some examples of these reactions and practical instructions. Most schools seem to have some of these floating around. See p. 196-201, with experiment 8.4b on p. 196. Summary chart taken from p. 201. The reaction to pro ...
... Nuffield Advanced Chemistry students book (I used fourth edition) is good, it has some examples of these reactions and practical instructions. Most schools seem to have some of these floating around. See p. 196-201, with experiment 8.4b on p. 196. Summary chart taken from p. 201. The reaction to pro ...
F.example
... Functional groups: Regions of molecules that have nonmetal atoms other than C and H or that have double or triple bonds are specific sites in organic molecules that chemicals most often attack. These small structural units are called functional groups, because they are the chemically functioning gro ...
... Functional groups: Regions of molecules that have nonmetal atoms other than C and H or that have double or triple bonds are specific sites in organic molecules that chemicals most often attack. These small structural units are called functional groups, because they are the chemically functioning gro ...
CH 12-3 Power Point
... •The 3-step series of reactions includes the unique reaction of an alkyl halide (R-X) with magnesium metal (Mg) to form a C-Mg “organic-metallic” bond: ...
... •The 3-step series of reactions includes the unique reaction of an alkyl halide (R-X) with magnesium metal (Mg) to form a C-Mg “organic-metallic” bond: ...
organic chem ppt notes
... ene for an alkene; in –yne for an alkyne. The position of the double or triple bond in the carbon chain is indicated by a number before the name of the chain. 2. Name the groups attached as in alkanes. ...
... ene for an alkene; in –yne for an alkyne. The position of the double or triple bond in the carbon chain is indicated by a number before the name of the chain. 2. Name the groups attached as in alkanes. ...
Alkene - Synthesis
... Acetone can dissolve both the iodide and the alkyl halide (if small). If Zn is used, reaction is heterogeneous and takes place on the surface of the Zn. Reduction because “Br2” is removed. ...
... Acetone can dissolve both the iodide and the alkyl halide (if small). If Zn is used, reaction is heterogeneous and takes place on the surface of the Zn. Reduction because “Br2” is removed. ...
12SN-23-10 OBJECTIVE: Identify how alcohols are classified and
... Identify how alcohols are classified and named. Predict how the solubility of an alcohol varies with the length of its carbon chain. Name the reactions of alkenes that may be used to introduce functional groups. Construct the general structure of an ether and describe how ethers are named. Identify ...
... Identify how alcohols are classified and named. Predict how the solubility of an alcohol varies with the length of its carbon chain. Name the reactions of alkenes that may be used to introduce functional groups. Construct the general structure of an ether and describe how ethers are named. Identify ...
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. ...
Assignment 2 Group A and B
... 9) Which of the following alcohols can be prepared by the reaction of methyl formate with excess Grignard reagent? A) 1-pentanol B) 2-pentanol C) 3-pentanol D) 2-methyl-2-pentanol E) 3-methyl-3-pentanol 10) What reagent(s) would you use to accomplish the following conversion? ...
... 9) Which of the following alcohols can be prepared by the reaction of methyl formate with excess Grignard reagent? A) 1-pentanol B) 2-pentanol C) 3-pentanol D) 2-methyl-2-pentanol E) 3-methyl-3-pentanol 10) What reagent(s) would you use to accomplish the following conversion? ...
Organic Chemistry Midterm Review Go over the Activities and
... 26. Draw alternative chair conformations and indicate the more stable one. ...
... 26. Draw alternative chair conformations and indicate the more stable one. ...
Mr. Farnworth
... • Carbon atom may also share two of its electrons with two from another atom to form an double bond. (up to three) • A carbon atom can never form more than a total of four bonds ...
... • Carbon atom may also share two of its electrons with two from another atom to form an double bond. (up to three) • A carbon atom can never form more than a total of four bonds ...
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.