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CHEM 122: Introduction to Organic Chemistry Chapter 9: Aldehydes
CHEM 122: Introduction to Organic Chemistry Chapter 9: Aldehydes

... a) Draw a structural formula for this cyclic hemiacetal. b) How many stereoisomers are possible for 5-hydroxyhexanal? c) How many stereoisomers are possible for this cyclic hemiacetal? 24. The following molecule is an enediol; each carbon of the double bond carries an –OH group. Draw structural form ...
Naming organic compounds
Naming organic compounds

... If there is more than one branch, the branches are identified in alphabetical order ignoring any di, tri etc. Be aware! Each branch needs to be numbered individually, even if they are attached to the same carbon atom. The rule is a comma between numbers and a dash between numbers and letters. ...
Chapter 2 Review Biopardy File
Chapter 2 Review Biopardy File

... A) Saturated fats have only single bonds B) Unsaturated fats have at least one double bond C) Unsaturated fats are good, saturated fats are bad D) All of the above are true ...
H - Frederick H. Willeboordse
H - Frederick H. Willeboordse

... However, this is not really the case. The six electrons of the Oxygen (repelling each other due to their equal charges) want to be as far from each other as possible. ...
The SN2 Reaction: 1
The SN2 Reaction: 1

... Introduction In this experiment 1-butanol is converted to 1-bromobutane by an SN2 reaction. In general, a primary alkyl bromide can be prepared by heating the corresponding alcohol with (1) constantboiling hydrobromic acid (47% HBr), (2) an aqueous solution of sodium bromide and excess sulfuric acid ...
Islamic University of Gaza Biochemistry School of Nursing Midterm
Islamic University of Gaza Biochemistry School of Nursing Midterm

... the four groups attached to them, lie in a single plane (incorrect) All four groups and the 2 carbon atoms lie in a single plane 9. A tertiary alcohol is one in which the –OH is attached to a carbon atom that has three or more carbon atoms attached to it. (incorrect) three 10. The product of the oxi ...
Course Syllabus - San Diego Mesa College
Course Syllabus - San Diego Mesa College

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Dr. Baxley`s Thermodynamics Worksheet
Dr. Baxley`s Thermodynamics Worksheet

... you would look at how many bonds are formed vs how many break) b. Using ∆G°f, I get −1226 kJ. Using ∆H°f and S°f, then ∆G° = ∆H°–T∆S°, I get –1227 kJ 6. Since formation of a bond has − ∆H° and − ∆S°, breaking of bonds has + ∆H° and + ∆S°. Putting this into the equation ∆G° = ∆H° − T∆S°, you get sign ...
ether - TeacherWeb
ether - TeacherWeb

with answers
with answers

... reaction proceeds. Why was it such a great challenge to develop an efficient industrial synthesis of ammonia, for which Carl Bosch obtained the Nobel Prize? N2 + 3 H2 2 NH3 The entropy decreases, as there are fewer gas molecules on the right-hand side. Very high activation energy, so rate of uncatal ...
Chap5
Chap5

... atoms, as is the case for alkanes. A prefix number is used to indicate the position of the carbon atom immediately before the double or triple bond, and a suffix (ene or yne) is used to indicate whether the compound is an alkene or an alkyne. 2) The chain is numbered so that the double/triple bond w ...
LOYOLA COLLEGE (AUTONOMOUS), CHENNAI – 600 034
LOYOLA COLLEGE (AUTONOMOUS), CHENNAI – 600 034

... 20. Explain Gabriel phthalimide synthesis. How would you use this method in the preparation of glycine and n-propyl amine? ...
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Chapter 10-

... Carbon forms stable, covalent bonds with other atoms such as H, O, N, S, and halogens ...
L 26 Hydrocarbons
L 26 Hydrocarbons

... CH3  Cl2   CH3Cl  Cl (iii) Chain Termination Step : In this step, free radicals combine with one another and the further reaction stops. ...
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Oxidation notes

... • Should have seen 3 peaks (one for each alkene product), BUT only see 2 peaks… – Poor resolution – “Missing” peak is actually covered up by large peak. ...
Review Sheet Chemistry II Final 2013
Review Sheet Chemistry II Final 2013

... Review Sheet Chemistry II Final 2013 Chapter 5 Atomic structure sample problems 1-3 Atom, electron, proton, neutron Diagram an atom Atomic number, atomic mass Ion, Cation, Anion, how is an ion formed Isotope, how to calculate average atomic mass Periodic Table metal, nonmetals, metalloids, noble gas ...
Alicyclic esters of phosphoric acids
Alicyclic esters of phosphoric acids

Study Materials
Study Materials

... 6. Application  of  organic  compounds  in  usage  of  drugs  in  the  field  of  medicine  has  given  rise  to  chemotherapy.    To  name  a  few,  dettol  (Chloro‐xylenol),  salol  are  antiseptics,  penicillin,  tetracycline  are  antibiotics,  aspirin,  despirin,  novalgin  which  reduce  pain  ...
Ppt09(Wk14)Organic_final_topics
Ppt09(Wk14)Organic_final_topics

... – Cis = “same side”; trans = “across from one another” ...
Ppt09(Wk14)Organic_final_topics
Ppt09(Wk14)Organic_final_topics

... • Ligands were either 90° (cis) or 180° (trans) apart from one another ...
2.10 Organic synthesis – Oxidation of alcohols
2.10 Organic synthesis – Oxidation of alcohols

... • The reaction will proceed at a constant temperature (i.e. the solvent's boiling point.). •Any vapours given off are cooled back to liquid, and fall back into the reaction vessel • Useful for performing chemical reactions under controlled conditions that require substantial time for completion. ...
HYDROCARBONS HYDROCARBONS Types of Hydrocarbons
HYDROCARBONS HYDROCARBONS Types of Hydrocarbons

... 8. Certain common nomenclatures are used in the IUPAC system ...
Organic Chemistry Fifth Edition
Organic Chemistry Fifth Edition

... A functional group is a structural unit in a molecule responsible for its characteristic physical properties as well as its behavior under a particular set of reaction conditions. Alkenes and alkynes are examples of functional groups. In this chapter we specifically meet alkylhalides and alcohols ...
Exam 1
Exam 1

... Acid catalyzed ester & amide hydrolysis, Fisher esterification, trans esterification Hydroxide promoted ester hydrolysis Nucleophilic addition to aldehyde/ketone with Grignard reagents Determine reaction mechanisms from reaction outcome (see Mechanism work sheet). Be able to recognize the following ...
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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.
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