Substituent PowerPoint Presentations - PPT

Aromatic Compounds Chapter 6
Aromatic Compounds Chapter 6 - presentation

tatiana-do

240 . Chem. 1. The expressing . aromatic compounds . came to mean . benzene. . and derivatives of benzene. .. . Structure of Benzene: Resonance Description. C. 6. H. 6. It contains a six-membered ring and three additional degrees of unsaturation..

substituent),NOandXOCl,Br,I)areexaminedintermsoftheirsources,interconv
substituent),NOandXOCl,Br,I)areexaminedintermsoftheirsources - pdf

liane-varn

Fig.1Thesources,interconversionsandsinksforHO(andRO)inthetroposphere. Table1Calculatedfractionalcontributionofvariousphotolysisratestoradicalproduction(OH)withaltitudeforcleanconditionsGround0.680.0Ne

Reaktionsmechanismen  Elektrophile
Reaktionsmechanismen Elektrophile - presentation

lindy-duni

aromatische Substitution. Additions-Eliminierungs-Mechanismus. Ausgangs- und Endverbindung sind aromatisch.. Zwischenstufe ist nicht aromatisch, die positive Ladung kann aber. mesomer. stabilisiert werden..

Saturated Hydrocarbons
Saturated Hydrocarbons - presentation

danika-pri

Alkanes. Dr. . Shatha. I . Alaqeel. 1. 108 . Chem. Learning Objectives. Chapter one discusses the following topics and the student by the end of this chapter will:. . Know the classification of hydrocarbon.

The name of every organic molecule has 3 parts:
The name of every organic molecule has 3 parts: - presentation

cheryl-pis

The . parent name . indicates the number of carbons in the . longest continuous chain. .. The . suffix. indicates what . functional group. is present.. The . prefix. tells us the identity, location, and number of substituents attached to the carbon chain..

Hydro
Hydro - presentation

lois-ondre

carbon. s are compounds that are only composed of . hydrogen. and . carbon. .. Which of the molecules above is saturated with hydrogen atoms?. 4.1 Alkanes. Copyright 2012 John Wiley & Sons, Inc..

Nomenclature Dr. Clower CHEM 2411
Nomenclature Dr. Clower CHEM 2411 - presentation

tatiana-do

Spring 2014. McMurry. (8. th. ed.) sections . 3.2, 3.3, 3.4, 4.1, 4.2, 7.3, 7.4, 9.1, 10.1, 15.1, 17.1,18.1, . 18.8, 19.1. , 20.1, 21.1, . 24.1, Appendix A. Nomenclature. The naming of organic molecules.

Organic Chemistry Structure
Organic Chemistry Structure - presentation

myesha-tic

Hydrocarbon: . A compound composed only of carbon and hydrogen.. Saturated hydrocarbon: . A hydrocarbon containing only single bonds.. Alkane:. A saturated hydrocarbon whose carbons are arranged in a open chain..

Chapter 2 Alkanes and Cycloalkanes;
Chapter 2 Alkanes and Cycloalkanes; - presentation

giovanna-b

Conformational and Geometrical Isomerism. Hydrocarbons. . are . compounds that contain only carbon and hydrogen. . There are three main classes of hydrocarbons, based on the types of carbon–carbon bonds present. .

Chapter 4- Alkanes
Chapter 4- Alkanes - presentation

yoshiko-ma

Hydrocarbons. Alkanes-. Alkenes-. Alkynes-. Cycloalkanes- . alkanes in which all or some of the carbon atoms are arranged in rings. General Formulas. Alkanes- C. n. H. 2n+2. Alkenes- C. n. H. 2n. Alkynes- C.

Chapter 17: Benzene and
Chapter 17: Benzene and - presentation

celsa-spra

Aromaticity. TNT. 8-methyl-N-vanillyl-6-nonenamide (. Capsaicin). Buckminsterfullerene. Key points & objectives:. Aromatic molecules are cyclic, conjugated, flat, and unusually stable. 4n + 2 electrons (.

Chapter 4- Alkanes Hydrocarbons
Chapter 4- Alkanes Hydrocarbons - presentation

tawny-fly

Alkanes-. Alkenes-. Alkynes-. Cycloalkanes- . alkanes in which all or some of the carbon atoms are arranged in rings. General Formulas. Alkanes- C. n. H. 2n 2. Alkenes- C. n. H. 2n. Alkynes- C. n. H.

1 Spectroscopy Introduction
1 Spectroscopy Introduction - presentation

conchita-m

2. UV Spectroscopy. Introduction. UV radiation and Electronic Excitations. The difference in energy between molecular bonding, non-bonding and anti-bonding orbitals ranges from 125-650 kJ/mole. This energy corresponds to EM radiation in the ultraviolet (UV) region, 100-350 nm, and visible (VIS) regions 350-700 nm of the spectrum.

Chapter 2 : Alkanes and Cycloalkanes
Chapter 2 : Alkanes and Cycloalkanes - presentation

celsa-spra

The Structure of Alkanes. Nomenclature of Organic Compounds. Alkyl groups. Numbering the parent carbon chain. The root name is that of the longest continuous carbon chain (. parent carbon chain. ) . Groups attached to the main chain are called .

Aromatic compounds
Aromatic compounds - presentation

ellena-man

Dr. . Sheppard. CHEM . 2412. Summer 2015. Klein (2. nd. ed. .) . sections. : 18.1, 18.2, 18.8, 18.3, 18.4, 18.5. Aromatic Compounds. Originally distinguished because of smell. Then noticed trends in reactivity.

Functional Groups
Functional Groups - presentation

kittie-lec

Functional Groups. Functional groups: special groups of atoms attached to a hydrocarbon skeleton; the most common sites of chemical reactivity.. Organic halides: . a hydrogen is replaced by a halogen.

Functional Groups
Functional Groups - presentation

myesha-tic

Functional Groups. Functional groups: special groups of atoms attached to a hydrocarbon skeleton; the most common sites of chemical reactivity.. Organic halides: . a hydrogen is replaced by a halogen.

Naming the Alkenes
Naming the Alkenes - presentation

yoshiko-ma

11-1. Alkenes are characterized by the presence of a double bond.. The general formula of an alkene is C. n. H. 2n. , the same as for a cycloalkane.. Common nomenclature for alkenes replaces the corresponding alkane suffix –ane with -ylene. .

12.3  Alkanes with Substituents
12.3 Alkanes with Substituents - presentation

briana-ran

When an alkane has four or more carbon atoms, the atoms can be arranged so that a side group called a . branch . or. . substituent. . . is attached to a carbon chain.. Learning Goal . . Write the IUPAC names for alkanes with substituents and draw their condensed and line-angle structural formulas. .

Organic and Inorganic Esters from Alcohols
Organic and Inorganic Esters from Alcohols - presentation

myesha-tic

9-4. Organic esters are derivatives of carboxylic acids.. Inorganic esters are the analogous derivatives of inorganic acids.. Organic and Inorganic Esters from Alcohols. 9-4. Alcohols react with carboxylic acids to give organic esters..

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