The IUPAC name of α–Farnesene including the stereochemistry is to be given. Concept introduction: The longest carbon chain containing the double bond to be chosen. Based on the name of the parent compound–the alkene name ends with the suffix–ene. The chain is to be numbered from the end that gives the lowest number to the carbon in double bond. Substituents are to be numbered according to their positions in the chain and listed alphabetically. The position of the double bond is indicated by giving the number of the first alkene carbon before the name of the parent name. If more than one double bond is present, their positions are indicated with the suffixes -diene, -triene and so on. The isomer that has the higher ranked groups on each carbon are on the same side of the double bond is said to have Z configuration. If the higher ranked groups are on opposite sides, the alkene is said to have E configuration. To give: The IUPAC name of α-farnesene including the stereochemistry.
The IUPAC name of α–Farnesene including the stereochemistry is to be given. Concept introduction: The longest carbon chain containing the double bond to be chosen. Based on the name of the parent compound–the alkene name ends with the suffix–ene. The chain is to be numbered from the end that gives the lowest number to the carbon in double bond. Substituents are to be numbered according to their positions in the chain and listed alphabetically. The position of the double bond is indicated by giving the number of the first alkene carbon before the name of the parent name. If more than one double bond is present, their positions are indicated with the suffixes -diene, -triene and so on. The isomer that has the higher ranked groups on each carbon are on the same side of the double bond is said to have Z configuration. If the higher ranked groups are on opposite sides, the alkene is said to have E configuration. To give: The IUPAC name of α-farnesene including the stereochemistry.
Solution Summary: The author explains the IUPAC name of –farnesene including the stereochemistry.
Definition Definition Organic compounds that contain at least one double bond between carbon-carbon atoms. The general molecular formula for alkenes with one double bond is C n H 2n .
Chapter 7.SE, Problem 41AP
Interpretation Introduction
Interpretation:
The IUPAC name of α–Farnesene including the stereochemistry is to be given.
Concept introduction:
The longest carbon chain containing the double bond to be chosen. Based on the name of the parent compound–the alkene name ends with the suffix–ene. The chain is to be numbered from the end that gives the lowest number to the carbon in double bond. Substituents are to be numbered according to their positions in the chain and listed alphabetically. The position of the double bond is indicated by giving the number of the first alkene carbon before the name of the parent name. If more than one double bond is present, their positions are indicated with the suffixes -diene, -triene and so on. The isomer that has the higher ranked groups on each carbon are on the same side of the double bond is said to have Z configuration. If the higher ranked groups are on opposite sides, the alkene is said to have E configuration.
To give:
The IUPAC name of α-farnesene including the stereochemistry.
The IUPAC name of the compound
H-
is
(a) 5-formylhex-2-en-3-one
(b) 5-methyl-4-oxohex-2-en-5-al
(c) 3-keto-2-methylhex-5-enal
(d) 3-keto-2-methylhex-4-enal (
The correct statement regarding electrophile is
(a) electrophile is a negatively charged species
and can form a bond by accepting a pair of
electrons from another electrophile
(b) electrophiles are generally neutral species
and can form a bond by accepting a pair of
electrons from a nucleophile
(c) electrophile can be either neutral or
ar positively charged species and can form a
bond by accepting a pair of electrons from
a nucleophile
(d) electrophile is a negatively charged species
and can form a bond by accepting a pair of
electrons from a nucleophile..
Which among the given molecules can exhibit
tautomerism?
Ph
Ph
I
II
III
(a) III only
(c) Both I and II
(b) Both I and III
(d) Both II and III
1)
Which of the following biphenyls is optically
active?
When the acyclic portion of the molecule contains more carbon atoms (or an important functional group), name
the ring as a cycloalkyl substituent.
(g)
xe
(1)
(h)
Give the common name for
NN
OH
T
CH3-CH₂-C-N-CH₂-CH3
Spell out the common name of the compound.
Give the IUPAC name for
0 CH₂
||
CH₂-C-N-CH₂-CH₂-CH₂,
Spell out the IUPAC name of the compound.
diethylamine
Draw all missing reactants and/or products in the appropriate boxes by placing atoms on the canvas and
connecting them with bonds. Add charges where needed.
HE CONT
HO