Organics Week 1 Flashcards
What are aldehydes?
Aldehydes are compounds that end with -al. They contain a carbonyl group (C=O) at the end of a carbon chain.
What are curly arrows and what do they show?
Curly arrows are used in reaction mechanisms to show the movement of electron pairs. They indicate the origin and final location of the electron pair involved in a reaction.
What are alkyl groups?
Alkyl groups are formed by removing one hydrogen from alkanes. They are represented by the prefix of the alkane name.
What are ketones?
Ketones are compounds that end with -one. They contain a carbonyl group (C=O) in the middle of a carbon chain.
What are esters?
Esters are formed from acids and alcohols. They are characterized by the presence of an ester group (-COO-) in the molecule.
What are alkanes?
Alkanes are compounds that end with -ane. They are hydrocarbons with only single carbon-carbon bonds (C-C).
What are alcohols?
Alcohols are compounds that end with -ol. They are characterized by a hydroxyl group (-OH) attached to a carbon atom.
What are nitriles?
Nitriles are compounds that end with -nitrile. They contain a cyano group (-CN) attached to a carbon atom.
What are amides?
Amides are compounds that contain the amide group (-CONH2). They are derived from carboxylic acids by replacing the hydroxyl group (-OH) with an amino group (-NH2).
What is the homologous series?
A homologous series is a family of hydrocarbons with similar chemical properties that share the same general formula. Each consecutive member of the series differs by CH2.
What are alkenes?
Alkenes are hydrocarbons that end with -ene. They contain at least one carbon-carbon double bond (C=C).
What are acid anhydrides?
Acid anhydrides are formed by dehydrating acids. They contain two carbonyl groups (C=O) attached to the same oxygen atom.
What is a hydrocarbon?
A hydrocarbon is a chemical compound composed solely of hydrogen and carbon atoms. It can be categorized into two primary categories: saturated hydrocarbons, which consist exclusively of single carbon-carbon bonds (C-C), and unsaturated hydrocarbons, which possess at least one double bond between carbon atoms (C=C).
What are acyl chlorides?
Acyl chlorides are compounds that end with -oyl chloride. They contain a carbonyl group (C=O) and a chlorine atom attached to a carbon atom.
What are amines?
Amines are compounds that contain the amino group (-NH2). They can be primary, secondary, or tertiary depending on the number of carbon groups attached to the nitrogen atom.
What are reaction mechanisms?
Reaction mechanisms show the reactions of organic compounds. They illustrate the step-by-step process of how reactants are transformed into products.
What are carboxylic acids?
Carboxylic acids are compounds that end with -oic acid. They contain a carboxyl group (-COOH) attached to a carbon atom.
In a reaction between ethene and hydrogen bromide, what happens to the carbon-carbon bond?
In a reaction between ethene and hydrogen bromide, the carbon-carbon bond breaks and the electron pair shifts to form a new bond with hydrogen.
What is the difference between saturated and unsaturated hydrocarbons?
Saturated hydrocarbons consist exclusively of single carbon-carbon bonds, while unsaturated hydrocarbons possess at least one double bond between carbon atoms.
What occurs in the subsequent step of the reaction involving a bromide ion?
In the subsequent step, a lone pair of electrons from the bromide ion relocates to create a bond with carbon, resulting in the formation of bromoethane.
How is the movement of electron pairs depicted in the reaction between ethene and hydrogen bromide?
The electrons from one of the carbon-carbon bonds shift to form a fresh bond with the hydrogen from HBr. Simultaneously, the electron pair in the hydrogen-bromine bond relocates to the bromine atom.
What are hydrocarbons and how are they categorized?
Hydrocarbons are chemical compounds composed of hydrogen and carbon atoms. They are categorized as saturated or unsaturated based on the presence of single or double carbon-carbon bonds.
How are acid anhydrides formed?
Acid anhydrides are formed by dehydrating acids, such as propanoic anhydride (C6H10O3).
What do curly arrows indicate in terms of electron pair movement?
Curly arrows indicate the starting point and final location of the electron pair.
How are alkyl groups formed?
Alkyl groups are formed by eliminating a hydrogen atom from alkanes.
What is chain isomerism?
Chain isomerism is a type of structural isomerism where compounds possess the same molecular formula but show differences in the arrangement of the carbon skeletons. This means that the carbon atoms are arranged in a different order in each isomer, resulting in different structural formulae.
What is position isomerism?
Position isomerism is a type of structural isomerism where compounds have the same molecular formula, but their structures differ due to the varying positions of a specific functional group within the same carbon skeleton. This means that the functional group is attached to different carbon atoms in each isomer, resulting in different structural formulae.
What is E-Z isomerism?
E-Z stereoisomerism is a type of stereoisomerism that occurs due to restricted rotation about the carbon-carbon double bond. It involves compounds with double bonds where two different groups or atoms are attached at both ends of the double bond.
What is cis-trans isomerism?
Cis-trans isomerism, also known as geometric isomerism, is a type of stereoisomerism that occurs when two groups or atoms are attached to the carbon atoms of a double bond and are arranged differently in space. In cis isomers, similar or identical groups are on the same side of the double bond, whereas in trans isomers, they are on opposite sides.
What is stereoisomerism?
Stereoisomerism is a type of isomerism observed in compounds with double carbon-carbon bonds, such as alkenes. Stereoisomers have identical structural formulae but differ in the spatial arrangement of their atoms.
What is isomerism?
Isomerism is a phenomenon in which compounds share the same molecular formula but have different structural or spatial arrangements. There are two main types of isomerism: structural isomerism and stereoisomerism.
What is functional group isomerism?
Functional group isomerism is a type of structural isomerism where compounds share a molecular formula but arrange their atoms differently to produce different functional groups. This means that the atoms are connected in a different way in each isomer, resulting in different structural formulae and different functional groups.
What is structural isomerism?
Structural isomerism is a type of isomerism where compounds have the same molecular formula but different structural arrangements or structural formulae. There are three common types of structural isomerism: chain isomerism, position isomerism, and functional group isomerism.
What does structural isomerism refer to?
Structural isomerism refers to compounds with the same molecular formula but different structural arrangements.
What is the effect of the arrangement of polar C-Cl bonds on the polarity of a molecule?
If the polar C-Cl bonds are arranged on one side of the molecule, it results in a partial negative charge on that side, making the molecule polar. If they are placed on opposite sides, the dipoles cancel each other out, making the molecule non-polar.