Question:
The term given to organic molecules which contain no multiple bonds.
Answer:
saturated
Related Questions & One-Liners
- An instrument used to measure the amount of rotation of plane polarized light by a compound, generally prepared in a solution
- A group that is used to protect a functional group from unwanted reactions. After application the protecting group can be removed to reveal the original functional group.
- An equimolar mixture of the two enantiomeric isomers of a compound.
- A a term applied to an atom or molecule having one or more free valencies.
- A chemical processes in which the proportion of more electronegative substituents is decreased, or the charge is made more negative, or the oxidation number is lowered.
- The process of separation of a racemate into its two enantiomers by means of some chiral agency.
- The representation of a compound by two or more canonical structures in which the valence electrons are rearranged to give structures of similar probability.
- A process in which the forward reaction can reach an equilibrium with the reverse reaction.
- Isomers formed by restricted rotation
- A formal non-ambiguous, nomenclature system for the assignment of absolute configuration of structure to chiral atoms, using the Cahn, Ingold and Prelog priority rules.
- An instrument that measures the spectrum of a sample.
- The sideways projection of a carbon-carbon single bond and the attached substituents.
- An instrument that measures the degree of absorption (or emission) of electromagnetic radiation by a substance.
- When a complex is formed between a metal ion and an a ligand in solution, the equilibrium may be expressed by a constant which is related to the free energy change for the process
- An instrument used to measure the amount of rotation of plane polarized light by a compound, generally prepared in a solution
- A group that is used to protect a functional group from unwanted reactions. After application the protecting group can be removed to reveal the original functional group.
- An equimolar mixture of the two enantiomeric isomers of a compound.
- A a term applied to an atom or molecule having one or more free valencies.
- A chemical processes in which the proportion of more electronegative substituents is decreased, or the charge is made more negative, or the oxidation number is lowered.
- The process of separation of a racemate into its two enantiomers by means of some chiral agency.
- The representation of a compound by two or more canonical structures in which the valence electrons are rearranged to give structures of similar probability.
- A process in which the forward reaction can reach an equilibrium with the reverse reaction.
- Isomers formed by restricted rotation
- A formal non-ambiguous, nomenclature system for the assignment of absolute configuration of structure to chiral atoms, using the Cahn, Ingold and Prelog priority rules.
- The term given to organic molecules which contain no multiple bonds.
- An instrument that measures the spectrum of a sample.
- The sideways projection of a carbon-carbon single bond and the attached substituents.
- An instrument that measures the degree of absorption (or emission) of electromagnetic radiation by a substance.
- When a complex is formed between a metal ion and an a ligand in solution, the equilibrium may be expressed by a constant which is related to the free energy change for the process
View All Questions
This question is a part of a larger set. Click the Link below to See all related questions.
Pharmaceutical Organic Chemistry One-Liners – Set 2
A set of essential Organic Chemistry one-liners to help pharmacy students reinforce key concepts quickly and prepare efficiently for exams.
View Complete Post ➔