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Lecture: 2 OCCURRENCE AND STRUCTURE OF
Lecture: 2 OCCURRENCE AND STRUCTURE OF

... The two families of monosaccharides, D-and L occur based on the configuration of D and L glyceraldehydes. In general, the D-family of sugars occur in nature.  For monosaccharides with two or more asymmetric carbons, the prefixes D or L refer to the configuration of the penultimate carbon (i.e, the ...
Chem 30BL * Lecture 2 - UCLA Chemistry and Biochemistry
Chem 30BL * Lecture 2 - UCLA Chemistry and Biochemistry

... the product because the reaction is carried out under thermodynamic conditions (elevated temperature) • The product distribution will change significantly if a different catalyst or different conditions are used for the reaction • Note also that only the five most abundant products (of nine products ...
Organic Chemistry 25.2 Introduction to Hydrocarbons
Organic Chemistry 25.2 Introduction to Hydrocarbons

enzymatic resolution of a racemic mixture by acylation in
enzymatic resolution of a racemic mixture by acylation in

Organic Chemistry Review
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... • You need to be able to recognize a alkane, alkene, or an alkyne by its chemical formula (Table Q). • Know how to use the general formulas, and know. They often ask this question as part of a substitution or addition reaction question. ...
Organic Chemistry Notes by Jim Maxka jim.maxka
Organic Chemistry Notes by Jim Maxka jim.maxka

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... Quaternary Carbon, 4°, = carbon attached to 4 other carbons, Very unreactive Hydrogens are classified based on carbon they are attached to – The hydrogens on a 1° carbon are called 1° hydrogens ...
CONDENSATION POLYMERS
CONDENSATION POLYMERS

Chapter 2: Nomenclature and Structure
Chapter 2: Nomenclature and Structure

... c. sec, iso indicate location of halogen d. methyl alcohol, isopropyl alcohol 2. IUPAC a. longest carbon chain containing the –OH functional grp b. suffix is “ol” instead of “ane” c. straight chains: number from side that gives lowest number to -OH d. where to put number i. can put it immediately be ...
Organic Synthesis
Organic Synthesis

... choice of starting materials is to work our way back from the target to simpler compounds. This is called retrosynthesis. We try to imagine what might have been the last step in the synthesis. The starting material for this reaction becomes our new target. What was the last step in its preparation? ...
Iodoform Test - organicchem.org
Iodoform Test - organicchem.org

... base and I2 lead to formation of the -triiodoketone. Hydroxide ion then reacts with the carbonyl carbon of the ketone in a nucleophilic acyl substitution, liberating iodoform (CHI3) from the reaction mixture. Iodoform is not soluble in the reaction conditions and precipitates, indicating the reacti ...
Elimination Reactions
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Answer Key for Final Exam

Hydrogenation catalysts from used nickel metal hydride batteries
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Study Guide Exam 2 and 3 Sp2011

... CH3CH2CH2CH2-O-CH2CH2CH2CH3 ...
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Forward

Procedure - organicchem.org
Procedure - organicchem.org

... base and I2 lead to formation of the -triiodoketone. Hydroxide ion then reacts with the carbonyl carbon of the ketone in a nucleophilic acyl substitution, liberating iodoform (CHI3) from the reaction mixture. Iodoform is not soluble in the reaction conditions and precipitates, indicating the reacti ...
Chemistry: The Central Science, 12e (Brown et al
Chemistry: The Central Science, 12e (Brown et al

... 25) The principal difference between fructose and glucose is that __________. A) fructose is a disaccharide and glucose is a monosaccharide B) fructose is a monosaccharide and glucose is a disaccharide C) fructose is chiral and glucose is not D) glucose is chiral and fructose is not E) fructose is a ...
crude oleoyl chloride
crude oleoyl chloride

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Nucleophilic Substitution Swapping

... The ability of solvents to stabilize ions through solvation is directly associated with their polarity. Polar solvents, such as water, can stabilize the ions 3X more than alcohol (see chart) Methanol can stabilize ions through solvation, but water is best at controlling ions. The :OH- is a super st ...
In the preparation of the esters given in this experiment
In the preparation of the esters given in this experiment

... 22. Give the structure and names of five alkenes having the molecular formula C6H12 that produce hexane on catalytic hydrogenation. 23. In an unsymmetrical alkene, the boron atom adds predominantly to the least substituted carbon atom. For example, 2-methyl-2-butene gives the products indicated in y ...
Chapter 14 – Aldehydes and Ketones
Chapter 14 – Aldehydes and Ketones

Chem 30BL_Lecture 2_.. - UCLA Chemistry and Biochemistry
Chem 30BL_Lecture 2_.. - UCLA Chemistry and Biochemistry

... the product because the reaction is carried out under thermodynamic conditions (elevated temperature) • The product distribution will change significantly if a different catalyst or different conditions are used for the reaction • Note also that only the five most abundant products (of nine products ...
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Alcohol



In chemistry, an alcohol is any organic compound in which the hydroxyl functional group (–OH) is bound to a saturated carbon atom. The term alcohol originally referred to the primary alcohol ethyl alcohol (ethanol), the predominant alcohol in alcoholic beverages.The suffix -ol appears in the IUPAC chemical name of all substances where the hydroxyl group is the functional group with the highest priority; in substances where a higher priority group is present the prefix hydroxy- will appear in the IUPAC name. The suffix -ol in non-systematic names (such as paracetamol or cholesterol) also typically indicates that the substance includes a hydroxyl functional group and, so, can be termed an alcohol. But many substances, particularly sugars (examples glucose and sucrose) contain hydroxyl functional groups without using the suffix. An important class of alcohols, of which methanol and ethanol are the simplest members is the saturated straight chain alcohols, the general formula for which is CnH2n+1OH.
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