Organic Chemistry Physical Properties. If the functional groups are the same, the length of the carbon chain tells us which organic compound will have.

Slides:



Advertisements
Similar presentations
Alcohols revisited (and ethers)
Advertisements

CI 13.2 – Alcohols and Ethers
Hydrocarbon Derivatives molecular compounds of carbon and hydrogen that contain at least one other element. ex) alkyl halide, alcohol, carboxylic acid,
Carbon Compounds Chapter 8 Section 2.
Organic Review.
Properties of Aldehydes and Ketones Chapter 13 Organic Compounds with oxygen and Sulfur.
Carboxylic Acids. A carboxylic acid contains a carboxyl group, which is a carbonyl group attach to a hydroxyl group. carbonyl group O  CH 3 — C—OH hydroxyl.
Aldehydes Ketones. Carbonyl group C = O Aldehydes Ketones Carboxylic acids Esters.
Properties of compounds
1 National 5 Chemistry Alcohols. 2 An alcohol contains  A hydroxyl group (—OH) attached to a carbon chain.
Chapter 12 Organic Compounds with Oxygen and Sulfur
Higher Chemistry Unit 2 Multiple Choice Questions Section 6 Esters
Physical and Chemical Properties Of Alcohols! By Joe Glenwright.
Organic chemistry is the branch of chemistry in which carbon compounds are studied.
Alcohols Lec.8. Introduction Alcohols have the general formula R-OH and are characterized by the presence of a hydroxyl group, -OH. They are structurally.
Amines, Aldehydes, Ketones
Functional Groups The great majority of organic compounds have C—C and C—H bonds. These are strong, non-polar bonds. They provide a non-reactive framework.
CHE 311 Organic Chemistry I Dr. Jerome K. Williams, Ph.D. Saint Leo University.
4.1 Systematic Nomenclature 1. Definitions Molecular formula Number of atoms in a molecule (element or compound) e.g. C 2 H 4 O 2 Empirical formula Simplest.
26-3: Carboxylic Acids and Esters
Carboxylic Acids and Esters,
Hydrocarbon Derivatives: Halocarbons Alcohols Ethers.
Organic Chemistry Functional Groups. The hydrocarbon skeleton of an organic molecule is chemically inert. Most organic chemistry, then, involves the atoms.
Hydrocarbon Derivatives:
Chapter 9 Aldehydes and Ketones Chemistry 20. Carbonyl group C = O Aldehydes Ketones Carboxylic acids Esters.
Alcohols, Ethers, Thiols and Chirality
Hydrocarbon Derivatives Chemistry 11. Hydrocarbon Derivatives Are formed when one or more hydrogen atoms is replaced by an element or a group of elements.
Organic Chemistry Larry Scheffler Lincoln High School Portland, OR.
An Introduction to Organic Chemistry. Orgins Originally defined as the chemistry of living materials or originating from living sources Wohler synthesized.
FUNCTIONAL GROUPS. A functional group is a cluster of atoms within a molecule that have specific reactivity patterns Compounds with the same functional.
Functional Groups.
Alcohols Similar to Hydrocarbons except for one group of chemicals. OH group. Hydroxyl group.
Hydrocarbon Derivatives:
Organic Chemistry Nathan Watson Lincoln High School Portland, OR.
Alcohols, Ethers, Thiols and Chirality
Organic Chemistry. Homologous Series A grouping of organic compounds based on their composition and properties A series has: A general formula The same.
Ch. 14: Carboxylic Acids, Esters, Amines and Amides
Introduction to Organic Chemistry Section Organic Chemistry The chemistry of carbon compounds Not including metal carbonates and oxides Are varied.
Bellringer/5.1 Notes 1.Name some similarities between the molecules of H 2 O and CO How are the molecules different? Study the models of the water.
Alcohols Alcohols Contain a hydroxyl group (-OH).
Organic Chemistry …oh what fun…. Organic Chemistry  What does it mean to be organic?  To be an organic compound means that you contain carbon … that’s.
Carbonyl Compounds We just keep going, and going, and going.
Leaving Certificate Chemistry
Amines and Amides.
Structure and Properties of Organic Molecules
Alcohols and Ethers Read pp
Leaving Certificate Chemistry
Chapter 16 Carboxylic Acids and Esters
Chapter 14 Aldehydes, Ketones, and Chiral Molecules
Hydrocarbons Functional Groups
Alcohols.
Chapter 13 Alcohols, Phenols, and Thiols
Chapter 16 Carboxylic Acids and Esters
Properties of compounds
Chapter 13 Alcohols, Phenols, and Thiols
Alcohols, Ethers, and Thiols
melting & boiling points
Structural Isomerism.
Trends in Physical Properties
Chapter 16 Carboxylic Acids and Esters
Biological Chemistry -- Organic: anything with carbon vs.
Lesson # 2: Functional Groups
Alcohols and Ethers AH Chemistry Unit 3(b).
Organic Chemistry An Introduction.
Chapter 10 Properties of Solids and Liquids
Biological Chemistry -- Organic: anything with carbon vs.
ALDEHYDES, KETONES AND CARBOXYLIC ACIDS
ALDEHYDES, KETONES AND CARBOXYLIC ACIDS
Chapter 14 Aldehydes, Ketones, and Chiral Molecules
Presentation transcript:

Organic Chemistry Physical Properties

If the functional groups are the same, the length of the carbon chain tells us which organic compound will have higher melting and boiling points. Longer carbon chain means higher melting and boiling points Reason: increasing the length of the non-polar chain increases the molar mass of the chain, which increases the strength of the dispersion forces between the molecules. Example: hexan-1-ol has higher melting and boiling points than ethanol NameStructural formulaMelting point (°C) Boiling point (°C) ethanolHO – CH 2 – CH hexan-1-olHO – CH 2 – CH 2 – CH 2 – CH 2 – CH 2 – CH

Physical Properties If the lengths of the carbon chain are similar, the polarity of the functional groups tells us which organic compound will have higher melting and boiling points. More polar groups means higher melting and boiling points Reason: more polar groups means stronger dipole-dipole forces between molecules Example: pentan-1-ol has higher melting and boiling points than pentanal Explanation: the O-H bond is more polar than the C=O bond. The pentan-1-ol will display hydrogen bonding between its molecules, pentanal will not. NameStructural formulaMelting point (°C) Boiling point (°C) pentanal H – C – CH 2 – CH 2 – CH 2 – CH pentan-1-ol HO – CH 2 – CH 2 – CH 2 – CH 2 – CH O

Physical Properties An isomeric acid of an ester is a carboxylic acid that has the same number of each element as the ester. (They have the same molecular formula.) Esters have lower boiling points than isomeric acids. Reason: The ester and its isomeric acid have the same length of non-polar carbon chain, so the boiling point depends on the polarity of the groups. Carboxylic acids contain a highly polar O-H bond so the molecules will display hydrogen bonding. The secondary interactions in the ester will be weaker. Example: pentanoic acid has a higher boiling point than ethyl propanoate (both have molecular formula C 5 H 10 O 2 ) NameStructural formulaBoiling point (°C) ethyl propanoate CH 3 – CH 2 – O – C – CH 2 – CH pentanoic acid HO – C – CH 2 – CH 2 – CH 2 – CH O O

Physical Properties In general, compounds with similar polarity dissolve each other (like dissolves like). Water is highly polar and displays hydrogen bonding between its molecules. Compounds with more polar groups and lower molar mass will be more soluble in water. Example:ethanol is more soluble in water than propanol (ethanol has a lower molar mass) Example:ethanol is more soluble in water than ethanal (a hydroxyl group is more polar than an aldehyde group) Example: butan-2,3-diol is more soluble than butan-2-ol (butan-2,3-diol has two hydroxyl groups, butan-2-ol only has one)