Intro to Naming Structures Flashcards
What is the IUPAC name for the following structure:
1-iodomethane
The prefix “meth” = 1 carbon
The common name would just be iodomethane
What is the IUPAC name for the following structure:
1-bromoethane
The prefix “eth” = 2 carbons
The common name is just bromoethane
What is the IUPAC name for the following structure:
1-fluoropropane
The prefix “prop” = 3 carbons
The common name is just fluoropropane
What is the IUPAC name for the following structure:
1-chlorobutane
The prefix “but” = 4 carbons
The common name is just chlorobutane
What is the IUPAC name for the following structure:
2-chloropropane
The common name is isopropyl chloride (the structure is a chlorine atom covalently bonded to the #2 carbon of an isopropyl group)
What is the IUPAC name for the following structure:
2-bromobutane
The common name is secbutyl bromide (the structure is a butyl group with a bromine substituent covalently bonded to the second carbon)
What is the IUPAC name for the following structure:
1-chloro-2,2-dimethylpropane
The common name is neopentyl chloride (the structure is a neopentyl group covalently bonded to chlorine at a terminal carbon)
What is the IUPAC name for the following structure:
1-iodo-2-methylbutane
The common name is isopropyl iodide (the structure is an isopropyl group covalently bonded to iodine at the #2 carbon)
What is the molecular/electronic geometry for the following molecule: H2C=O
What are the hybridization states for each atom? (besides H)
Also, note the bond angles around the central atom
The molecular and electronic geometries of this molecule are trigonal planar due to the sp2 hybridization of the carbon atom, giving bond angles of 120 degrees.
What is the molecular/electronic geometry for the following molecule: CH3+, why is this important when considering the stereoselectivity of certain reactions?
What are the hybridization states of the atoms? (Besides H)
The molecular and electronic geometries of this molecular are trigonal planar. This is due to the sp2 hybridization state (remember that + charges DO NOT count as a group when determining the hybridization state) of the central carbon atom, giving bond angles of 120 degrees. This allows for a nucleophile to approach the localized charge from either face, resulting in the racemization of the products.
What does the Greek prefix “prop-“ signify in organic chemistry?
Three carbons
What does the Greek prefix “pent-“ signify in organic chemistry?
Five carbons
What does the Greek prefix “meth-“ signify in organic chemistry?
One carbon
What does the Greek prefix “but-“ signify in organic chemistry?
Four carbons
What does the Greek prefix “nona-“ signify in organic chemistry?
Nine carbons