Ch. 6 - Thermodynamics and KineticsWorksheetSee all chapters
All Chapters
Ch. 1 - A Review of General Chemistry
Ch. 2 - Molecular Representations
Ch. 3 - Acids and Bases
Ch. 4 - Alkanes and Cycloalkanes
Ch. 5 - Chirality
Ch. 6 - Thermodynamics and Kinetics
Ch. 7 - Substitution Reactions
Ch. 8 - Elimination Reactions
Ch. 9 - Alkenes and Alkynes
Ch. 10 - Addition Reactions
Ch. 11 - Radical Reactions
Ch. 12 - Alcohols, Ethers, Epoxides and Thiols
Ch. 13 - Alcohols and Carbonyl Compounds
Ch. 14 - Synthetic Techniques
Ch. 15 - Analytical Techniques: IR, NMR, Mass Spect
Ch. 16 - Conjugated Systems
Ch. 17 - Aromaticity
Ch. 18 - Reactions of Aromatics: EAS and Beyond
Ch. 19 - Aldehydes and Ketones: Nucleophilic Addition
Ch. 20 - Carboxylic Acid Derivatives: NAS
Ch. 21 - Enolate Chemistry: Reactions at the Alpha-Carbon
Ch. 22 - Condensation Chemistry
Ch. 23 - Amines
Ch. 24 - Carbohydrates
Ch. 25 - Phenols
Ch. 26 - Amino Acids, Peptides, and Proteins

Solution: For the following, circle the capitalized word that best completes the statement.In general, it is best to think of alkenes and alkynes as NUCLEOPHILES or ELECTROPHILES that react with NUCLEOPHILES or ELECTROPHILES.In general, NUCLEOPHILES or ELECTROPHILES serve as electron sources and NUCLEOPHILES or ELECTROPHILES serve as electron sinks for most reactions.A pi bond or lone pair will serve as an ELECTRON SOURCE or ELECTRON SINK for an arrow that indicates the making of a new bond.An atom that can accommodate a new bond can serve as an ELECTRON SOURCE or ELECTRON SINK for an arrow that indicates the making of a new bond.A reaction that occurs faster (greater opportunity) has a LOWER or HIGHER activation energy.A reation that has a strong thermodynamic driving force (a strong motive) is FAVORABLE or UNFAVORABLE as written.

Problem

For the following, circle the capitalized word that best completes the statement.

In general, it is best to think of alkenes and alkynes as NUCLEOPHILES or ELECTROPHILES that react with NUCLEOPHILES or ELECTROPHILES.

In general, NUCLEOPHILES or ELECTROPHILES serve as electron sources and NUCLEOPHILES or ELECTROPHILES serve as electron sinks for most reactions.

A pi bond or lone pair will serve as an ELECTRON SOURCE or ELECTRON SINK for an arrow that indicates the making of a new bond.

An atom that can accommodate a new bond can serve as an ELECTRON SOURCE or ELECTRON SINK for an arrow that indicates the making of a new bond.

A reaction that occurs faster (greater opportunity) has a LOWER or HIGHER activation energy.

A reation that has a strong thermodynamic driving force (a strong motive) is FAVORABLE or UNFAVORABLE as written.