logo course lecturer : jasmin Šutković 28 th november 2015 organic chemistry – fall 2015 lecture...

52
LOGO Course lecturer : Jasmin Šutković 28 th November 2015 Organic Chemistry – FALL 2015 Lecture 3 : Introduction to Organic Chemistry

Upload: samantha-douglas

Post on 18-Jan-2016

216 views

Category:

Documents


0 download

TRANSCRIPT

Page 1: LOGO Course lecturer : Jasmin Šutković 28 th November 2015 Organic Chemistry – FALL 2015 Lecture 3 : Introduction to Organic Chemistry

LOGO

Course lecturer :

Jasmin Šutković

28th November 2015

Organic Chemistry – FALL 2015

Lecture 3 :Introduction to Organic Chemistry

Page 2: LOGO Course lecturer : Jasmin Šutković 28 th November 2015 Organic Chemistry – FALL 2015 Lecture 3 : Introduction to Organic Chemistry

Contents International University of Sarajevo

11.1 Introduction to Organic Chemistry11.2 Characteristic Features of OrganicCompounds11.3 Shapes of Organic Molecules11.4 Drawing Organic Molecules11.5 Functional Groups11.6 Properties of Organic Compounds11.7 FOCUS ON HEALTH & MEDICINE:Vitamins

Book chapter 11

Page 3: LOGO Course lecturer : Jasmin Šutković 28 th November 2015 Organic Chemistry – FALL 2015 Lecture 3 : Introduction to Organic Chemistry

Introduction

In this lecture we learn about the characteristic features of organic molecules.

What is organic chemistry?

Organic chemistry is the study of compounds that contain the element carbon.

Page 4: LOGO Course lecturer : Jasmin Šutković 28 th November 2015 Organic Chemistry – FALL 2015 Lecture 3 : Introduction to Organic Chemistry

Clothes, foods, medicines, gasoline, refrigerants, and soaps are composed almost solely of organic compounds.

Some, like cotton, wool, or silk are naturally occurring; that is, they can be isolated directly from natural sources.

Page 5: LOGO Course lecturer : Jasmin Šutković 28 th November 2015 Organic Chemistry – FALL 2015 Lecture 3 : Introduction to Organic Chemistry
Page 6: LOGO Course lecturer : Jasmin Šutković 28 th November 2015 Organic Chemistry – FALL 2015 Lecture 3 : Introduction to Organic Chemistry

We will start with smaller molecules, small number of C atoms.

Mehane (CH4) and Ethanol (C2H5OH)

Ethanol produced in Lab, Methane naturally.

CHARACTERISTIC FEATURES OF ORGANIC COMPOUNDS

Page 7: LOGO Course lecturer : Jasmin Šutković 28 th November 2015 Organic Chemistry – FALL 2015 Lecture 3 : Introduction to Organic Chemistry

All organic compounds contain carbon atoms and most contain hydrogen atoms. Carbon always forms four covalent bonds, and hydrogen forms one covalent bond.

Page 8: LOGO Course lecturer : Jasmin Šutković 28 th November 2015 Organic Chemistry – FALL 2015 Lecture 3 : Introduction to Organic Chemistry

Common fetures ?

Page 9: LOGO Course lecturer : Jasmin Šutković 28 th November 2015 Organic Chemistry – FALL 2015 Lecture 3 : Introduction to Organic Chemistry

Bonding depends on the atom number around C

Page 10: LOGO Course lecturer : Jasmin Šutković 28 th November 2015 Organic Chemistry – FALL 2015 Lecture 3 : Introduction to Organic Chemistry
Page 11: LOGO Course lecturer : Jasmin Šutković 28 th November 2015 Organic Chemistry – FALL 2015 Lecture 3 : Introduction to Organic Chemistry
Page 12: LOGO Course lecturer : Jasmin Šutković 28 th November 2015 Organic Chemistry – FALL 2015 Lecture 3 : Introduction to Organic Chemistry
Page 13: LOGO Course lecturer : Jasmin Šutković 28 th November 2015 Organic Chemistry – FALL 2015 Lecture 3 : Introduction to Organic Chemistry

The most common multiple bond between C and a heteroatom is carbon – oxygen double bond.

Carbon forms 4 stable bonds with itself and other elements. Carbon atoms bind together to fotm RINGS or CHAINS

Page 14: LOGO Course lecturer : Jasmin Šutković 28 th November 2015 Organic Chemistry – FALL 2015 Lecture 3 : Introduction to Organic Chemistry

Shapes of Organic molecules

Recall section 4.6 = the most stable structural arranement keeps its groups as far away from each other = VSEPR theory

Page 15: LOGO Course lecturer : Jasmin Šutković 28 th November 2015 Organic Chemistry – FALL 2015 Lecture 3 : Introduction to Organic Chemistry
Page 16: LOGO Course lecturer : Jasmin Šutković 28 th November 2015 Organic Chemistry – FALL 2015 Lecture 3 : Introduction to Organic Chemistry
Page 17: LOGO Course lecturer : Jasmin Šutković 28 th November 2015 Organic Chemistry – FALL 2015 Lecture 3 : Introduction to Organic Chemistry

All carbons having 4 single bonds are tetrahedral ! Exp : ethane

Page 18: LOGO Course lecturer : Jasmin Šutković 28 th November 2015 Organic Chemistry – FALL 2015 Lecture 3 : Introduction to Organic Chemistry

IUPAC name : ETHYNE = C2H2

IUPAC name : ETHENE = C2H4

Page 19: LOGO Course lecturer : Jasmin Šutković 28 th November 2015 Organic Chemistry – FALL 2015 Lecture 3 : Introduction to Organic Chemistry
Page 20: LOGO Course lecturer : Jasmin Šutković 28 th November 2015 Organic Chemistry – FALL 2015 Lecture 3 : Introduction to Organic Chemistry

Drawing organic molecules

Because organic molecules contain many atoms we need to find the best way to simplify their strucures.

TWO ways are used :

Condensed structures and Skeleton structures

• Condensed structures used for molecules having a chain of atoms bound together, rather than a ring.

• Skeleton structures used for molecules having a both, chain and ring of atoms.

Page 21: LOGO Course lecturer : Jasmin Šutković 28 th November 2015 Organic Chemistry – FALL 2015 Lecture 3 : Introduction to Organic Chemistry

Condensed structures

Following rules are used :

Page 22: LOGO Course lecturer : Jasmin Šutković 28 th November 2015 Organic Chemistry – FALL 2015 Lecture 3 : Introduction to Organic Chemistry

Skeletal structures

Page 23: LOGO Course lecturer : Jasmin Šutković 28 th November 2015 Organic Chemistry – FALL 2015 Lecture 3 : Introduction to Organic Chemistry

Functional groups

More than 20 milion organic compounds are known, most of the have C, H and O atoms.

Many organic molecules have also other structural feautures – called functional groups !

Page 24: LOGO Course lecturer : Jasmin Šutković 28 th November 2015 Organic Chemistry – FALL 2015 Lecture 3 : Introduction to Organic Chemistry

Functional group determines the molecule shape and therefore its function !

Functional group in this case in OH (hydroxyl group)

Page 25: LOGO Course lecturer : Jasmin Šutković 28 th November 2015 Organic Chemistry – FALL 2015 Lecture 3 : Introduction to Organic Chemistry
Page 26: LOGO Course lecturer : Jasmin Šutković 28 th November 2015 Organic Chemistry – FALL 2015 Lecture 3 : Introduction to Organic Chemistry

Hydrocarbons

Are organic molecules that contain only C and H elements.

Alkanes – single bonds Alkenes – double bond Alkynes – triple bond Aromatic hydrocarbons – benzane ring (6 C

atoms and 3 double bonds )

Page 27: LOGO Course lecturer : Jasmin Šutković 28 th November 2015 Organic Chemistry – FALL 2015 Lecture 3 : Introduction to Organic Chemistry
Page 28: LOGO Course lecturer : Jasmin Šutković 28 th November 2015 Organic Chemistry – FALL 2015 Lecture 3 : Introduction to Organic Chemistry

All hydrocarbons other than Alkanes contain multiple bonds. Alkanes, which have no functional groups and therefore no reactive sites, are notoriously uncreative except under very drastic conditions.

For example, polyethylene is a synthetic plastic and high molecular weight Alkane, consisting of long chains of CH2 groups bonded together, hundreds or even thousands of atoms long.

Page 29: LOGO Course lecturer : Jasmin Šutković 28 th November 2015 Organic Chemistry – FALL 2015 Lecture 3 : Introduction to Organic Chemistry

Polyethylene

Hydrocarbons that have NO other functional groups – no reactive sites are very UNREACTIVE in nature.

Exp :Polyethylene

Page 30: LOGO Course lecturer : Jasmin Šutković 28 th November 2015 Organic Chemistry – FALL 2015 Lecture 3 : Introduction to Organic Chemistry

COMPOUNDS CONTAINING A SINGLE BOND TO A HETEROATOM

Several types of functional groups contain a carbon atom singly bonded to a heteroatom.

Common examples include alkyl halides, alcohols, ethers, and amines, as shown in Table 11.4.

Page 31: LOGO Course lecturer : Jasmin Šutković 28 th November 2015 Organic Chemistry – FALL 2015 Lecture 3 : Introduction to Organic Chemistry
Page 32: LOGO Course lecturer : Jasmin Šutković 28 th November 2015 Organic Chemistry – FALL 2015 Lecture 3 : Introduction to Organic Chemistry

Molecules containing these functional groups may be simple or very complex. It doesn’t matter what else is present in other parts of the molecule.

Always dissect it into small pieces to identify the functional groups.

For example, diethyl ether, the first general anesthetic, is an ether because it has an O atom bonded to two C’s.

Page 33: LOGO Course lecturer : Jasmin Šutković 28 th November 2015 Organic Chemistry – FALL 2015 Lecture 3 : Introduction to Organic Chemistry

Tetrahydrocannabinol (THC), the active component in marijuana, is also an ether because it contains an O atom bonded to two carbon atoms. In this case the O atom is also part of a ring.

Page 34: LOGO Course lecturer : Jasmin Šutković 28 th November 2015 Organic Chemistry – FALL 2015 Lecture 3 : Introduction to Organic Chemistry

COMPOUNDS CONTAINING A C=O GROUP

Many different kinds of compounds contain a carbon–oxygen double bond (C=O, carbonyl group), as shown in Table 11.5.

Carbonyl compounds include aldehydes, ketones, carboxylic acids, esters, and amides. The type of atom bonded to the carbonyl carbon—hydrogen, carbon, or a heteroatom—determines the specific c class of carbonyl compound.

Page 35: LOGO Course lecturer : Jasmin Šutković 28 th November 2015 Organic Chemistry – FALL 2015 Lecture 3 : Introduction to Organic Chemistry
Page 36: LOGO Course lecturer : Jasmin Šutković 28 th November 2015 Organic Chemistry – FALL 2015 Lecture 3 : Introduction to Organic Chemistry

Aldehydes, Carboxylic acid and Esters

Page 37: LOGO Course lecturer : Jasmin Šutković 28 th November 2015 Organic Chemistry – FALL 2015 Lecture 3 : Introduction to Organic Chemistry
Page 38: LOGO Course lecturer : Jasmin Šutković 28 th November 2015 Organic Chemistry – FALL 2015 Lecture 3 : Introduction to Organic Chemistry

PROPERTIES OF ORGANIC COMPOUNDS

Because organic compounds are composed of covalent bonds, their properties differ a great deal from those of ionic inorganic compounds.

This causes lower melting points to organic molecules, many organic molecules are liquid (some gaseous) in rooms temperature (ionic molecules are solid)

Page 39: LOGO Course lecturer : Jasmin Šutković 28 th November 2015 Organic Chemistry – FALL 2015 Lecture 3 : Introduction to Organic Chemistry
Page 40: LOGO Course lecturer : Jasmin Šutković 28 th November 2015 Organic Chemistry – FALL 2015 Lecture 3 : Introduction to Organic Chemistry

POLARITY

Are organic compounds polar or nonpolar ?

That depends.

Like other covalent compounds, the polarity of an organic compound is determined by two factors:

the polarity of the individual bonds and the overall shape of the molecule.

The polarity of an individual bond depends on the electronegativity of the atoms that form it.

Page 41: LOGO Course lecturer : Jasmin Šutković 28 th November 2015 Organic Chemistry – FALL 2015 Lecture 3 : Introduction to Organic Chemistry
Page 42: LOGO Course lecturer : Jasmin Šutković 28 th November 2015 Organic Chemistry – FALL 2015 Lecture 3 : Introduction to Organic Chemistry
Page 43: LOGO Course lecturer : Jasmin Šutković 28 th November 2015 Organic Chemistry – FALL 2015 Lecture 3 : Introduction to Organic Chemistry
Page 44: LOGO Course lecturer : Jasmin Šutković 28 th November 2015 Organic Chemistry – FALL 2015 Lecture 3 : Introduction to Organic Chemistry

SOLUBILITY

Understanding the solubility properties of organic compounds allows us to understand many interesting phenomena.

One rule governs solubility: “Like dissolves like.”

Three facts can then be used to explain the solubility of organic compounds :

Page 45: LOGO Course lecturer : Jasmin Šutković 28 th November 2015 Organic Chemistry – FALL 2015 Lecture 3 : Introduction to Organic Chemistry

Three compounds—hexane, ethanol, and cholesterol—illustrate these principles. All of these compounds are organic and therefore soluble in an organic solvent like diethyl ether (CH3CH2OCH2CH3).

Their water solubility depends on their polarity and size.

Since hexane (CH3CH2CH2CH2CH2CH3) is a nonpolar hydrocarbon, it is insoluble in water.

Ethanol (CH3CH2OH), on the other hand, is water soluble because it is small and contains a polar OH group.

Page 46: LOGO Course lecturer : Jasmin Šutković 28 th November 2015 Organic Chemistry – FALL 2015 Lecture 3 : Introduction to Organic Chemistry

FOCUS ON HEALTH & MEDICINE

Vitamins

Vitamins are organic compounds needed in small amounts for normal cell function.

Our bodies cannot synthesize these compounds, so they must be obtained in our diet. Most vitamins are identified by a letter, such as A, C, D, E, and K. There are several different B vitamins, though, so a subscript is added to distinguish them—for example, B1, B2, and B12.

Vitamins are classified on the basis of their solubility properties.

Page 47: LOGO Course lecturer : Jasmin Šutković 28 th November 2015 Organic Chemistry – FALL 2015 Lecture 3 : Introduction to Organic Chemistry

Vitamin A

Vitamin A, or retinol, is an essential component of the vision receptors in the eyes.

It also helps to maintain the health of mucous membranes and the skin, so many anti-aging creams contain vitamin A.

A deficiency of this vitamin leads to a loss of night vision.

Page 48: LOGO Course lecturer : Jasmin Šutković 28 th November 2015 Organic Chemistry – FALL 2015 Lecture 3 : Introduction to Organic Chemistry
Page 49: LOGO Course lecturer : Jasmin Šutković 28 th November 2015 Organic Chemistry – FALL 2015 Lecture 3 : Introduction to Organic Chemistry

Vitamin C

Although most animal species can synthesize vitamin C, humans, some animals obtain this vitamin from dietary sources.

Citrus fruits, strawberries, tomatoes, and sweet potatoes are all excellent sources of vitamin C.

Vitamin C, or ascorbic acid, is important in the formation of collagen, a protein that forms the connective tissues of skin, muscle, and blood vessels.

A deficiency of vitamin C causes scurvy, a common disease of sailors in the 1600s who had no access to fresh fruits on long voyages.

Page 50: LOGO Course lecturer : Jasmin Šutković 28 th November 2015 Organic Chemistry – FALL 2015 Lecture 3 : Introduction to Organic Chemistry
Page 51: LOGO Course lecturer : Jasmin Šutković 28 th November 2015 Organic Chemistry – FALL 2015 Lecture 3 : Introduction to Organic Chemistry
Page 52: LOGO Course lecturer : Jasmin Šutković 28 th November 2015 Organic Chemistry – FALL 2015 Lecture 3 : Introduction to Organic Chemistry

Readings

Book Chapter 11

Book Page : 322-354