1. T OPIC 1: O RGANIC C OMPOUNDS : A LKANES AND C YCLOALKANES According to Chemical Abstracts, there are more than 18 million known organic compounds, each of which has its own physical properties, such as melting point and boiling point, as well as its own reactivity. Chemists have learned that organic compounds can be classified into families according to their structural features and that members of a given family often have similar chemical behavior. Instead of 18 million compounds with random reactivity, there are a few dozen families of organic compounds whose chemistry is reasonably predictable. Throughout this course, we will study the chemistry of specific families.

2. I.F UNCTIONAL G ROUPS  FUNCTIONAL GROUP: -Group of atoms within a molecule that has a characteristic chemical behavior - Behaves nearly the same way in every molecule

5. Caffeine Prozac Acetominophen Vanillin

6. Taxol, isolated from the bark of the Pacific Yew tree, Taxus brevifolia, is an anticancer drug, which was first studied in the successful treatment of ovarian cancer. In 1969, 1,200 kg of tree bark was processed to produce 10.0 g of pure taxol. The molecule contains 14 functional groups. Taxol

7. Since it would be impractical to harvest enough trees to obtain significant amounts of taxol, a semi-synthetic method was developed. Needles are harvested from a related, low growing evergreen, Taxus baccata, which is grown in plantations similar to growing tea. The needles are processed to produce large amounts of a synthetic precursor 10- deacetylbaccatin whose structure is shown below. 10- deacetylbaccatin -Synthetic precursor to taxol -More readily available

8. II. A LKANES AND A LKANE I SOMERS * You saw in Background Unit One that carbon-carbon single bonds result from head-on overlap of carbon sp 3 hybridized orbitals. One of the unique properties of carbon is its ability to bond to multiple carbon atoms results in long chains of atoms and the formation of complex molecules.

9.  ALKANES: -contain single carbon to carbon bonds -hydrocarbons: contain only C & H atoms -saturated: contain the max. number of H atoms per C atom -have the general formula: C n H 2n+2 (n = any integer) -nonpolar  STRAIGHT-CHAIN or NORMAL ALKANES: -carbons atoms are connected in a row -Ex.  BRANCHED-CHAIN ALKANES: -carbons atoms branch from the main chain -Ex.

10.  CONSTITUTIONAL ISOMERS: -contain the same number & types of atoms but differ in the way the atoms are arranged - have different chemical and physical properties Isomer Possibilities:

11. * Also remember that carbon- carbon single bonds can rotate. What may at first seem like two different molecules may really just be the same molecule represented in two different ways.

12. III. N AMING A LKANES * In earlier times when relatively few pure organic molecules were known, new compounds were named at the whim of their discoverer. Thus, urea (CH 4 N 2 O) is a crystalline substance isolated from urine; morphine (C 17 H 19 NO 3 ) is a painkiller named after Morpheus, the Greek god of dreams; and barbituric acid is a tran- quilizing agent named by its discoverer in honor of his friend Barbara. As the number of known organic compounds slowly grew, so did the need for a systematic way of naming them. Although many “common” naming for organic compounds still exist, the system of naming we used is devised by the International Union of Pure and Applied Chemistry (IUPAC, usually spoken as “eye-you-pac).

13. A chemical name in the IUPAC system has three parts: prefix parent suffix Where are the substituents? How many carbons? What is the main functional group present?

14. Naming Alkanes The names of alkanes are derived from a set of prefixes, used to indicate the number of carbons present PrefixFormulaPrefixFormula C1C1 C6C6 C2C2 C7C7 C3C3 C8C8 C4C4 C9C9 C5C5 C 10 meth- eth- prop- but- pent- hex- hept- oct- non- dec- The names of alkanes end in -ANE YOU MUST KNOW THESE!

15. Practice: Name the following alkanes

16. IV. P ROPERTIES AND R EACTIONS OF A LKANES * Alkanes are sometimes referred to as “paraffins”- a word derived from the Latin parum affinis, meaning “slight affinity.” This term aptly describes their behavior because alkanes show little affinity for other some substances and are, for the most part, chemically unreactive.

17. PROPERTY 1: ALKANES SHOW REGULAR INCREASES IN BOILING & MELTING POINTS AS THEIR MOLECULAR WEIGHT INCREASES -Due to van der Waals forces: weak intermolecular forces that operate over small distances & occur because the electron distribution in the molecules are non-uniform at any given instant & create temporary dipoles Bigger molecules = stronger temporary dipoles = more energy (higher temps.) needed to break the van der Waals forces

18. PROPERTY 2: INCREASED BRANCHING LOWERS AN ALKANES BOILING POINT -Branched-chain alkanes are more spherical, have smaller surface areas, and therefore have weaker van der Waals forces - Weaker van der Waals forces = lower boiling point

19. REACTION 1: COMBUSTION -When hydrocarbons burn in the presence of O 2, the products are H 2 O and CO 2 -A lot of heat is produced -Ex. CH 4 + O 2  CO 2 + H 2 O

20. REACTION 2: RADICAL HALOGENATION -Mixture of alkane and X 2 is irradiated w/ ultraviolet light (denoted as hυ) forming the X radical (odd electron species) -Products contain a variety of halogen substituted products -Cons of reaction: difficult to control the exact spot of halogenation (see example below) & mixtures of products form

21. V. C YCLOALKANES  CYCLOALKANES: -also called cyclic compounds -consist of rings of – CH 2 – units -have the general formula: C n H 2n The general class of compounds known as steroids contain four rings joined together- three of them six-membered rings and one of them a five membered ring. Cortisol, also known as hydrocortisone, an over the counter medicine used to treat skin irritations. Cholesterol is essential for all animal life. Each cell synthesizes it from simpler molecules, a complex 37-step process.

22. VI. C IS -T RANS I SOMERISM IN C YCLOALKANES * In many ways, cycloalkanes behave similar to their open- chain counterparts. One difference is that cycloalkanes are less flexible. In smaller rings (C 3 – C 6 ), rotation about the C – C bond is impossible. This leads to the ring having a “top” and a “bottom” side.

23.  STEREOISOMERS: -atoms are connected in the same order but differ in their spatial orientation  CIS –TRANS ISOMERS: -a special type of stereoisomers -cis: means groups are on the same side -trans: means groups are on the opposite side

24. A. 1,4- dimethylcyclohexane B. 1-methyl-3-propylcyclopentane C. 3-cyclobutylpentane D. 1-bromo-4-ethylcyclodecane E. 1-chloro-3-ethyl-2-methylcyclopentane F. 1-bromo-3-ethyl-5-propylcyclohexane G. 1-fluoro-2-methylcyclobutane H. 1-ethyl-4-methylcycloheptane I. 1,1,4-trimethylcyclohexane J. 3-cyclopentylheptane K. 1,3-dimethylcyclopentane L. 1-ethyl-2,2,6,6-tetramethylcyclohexane

25. A. 3-ethyl-4-methylhexane B. 4-ethyl-5,6-dimethyl-7-propyldecane C. 3,4,5-triethyl-6-methyloctane D. 3,4-diethyl-2-methylhexane E. 1,2-diethyl-3-methylcyclohexane F. 1,4-dibromo-2-fluorocyclopentane G. 1-cyclopropyl-2-propylcyclopentane H. 2-cyclopentyl-6-methyloctane I. 5-ethyl-3-methyl-6-propylnonane