
Concept explainers
(a)
Interpretation: Primary, secondary and tertiary hydrogen in below structure along with IUPAC name should be labeled.
Concept introduction: In accordance with IUPAC convention longest chain can be found from either direction provided it is longest and digits indicate the position of carbon or the position of branched alkyl chain in cases of branched hydrocarbons. All the side chains are named in alphabetical order.
The IUPAC system for nomenclature of straight hydrocarbon makes use of table given as follows:
Beside the IUPAC names there are certain common names. The common prefixes include prefixes “iso-” and “neo-”. For example, isobutane is common name used popularly for
The carbon linked to one alkyl/carbon while other two
The carbon linked to two alkyl /carbons and one
The carbon linked to three alkyl groups/carbons and no
These are indicated below:
(b)
Interpretation: Primary, secondary and tertiary hydrogen in below structure along with IUPAC name should be labeled.
Concept introduction: In accordance with IUPAC convention longest chain can be found from either direction provided it is longest and digits indicate the position of carbon or the position of branched alkyl chain in cases of branched hydrocarbons. All the side chains are named in alphabetical order.
The IUPAC system for nomenclature of straight hydrocarbon makes use of table given as follows:
Beside the IUPAC names there are certain common names. The common prefixes include prefixes “iso-” and “neo-”. For example, isobutane is common name used popularly for
The carbon linked to one alkyl/carbon while other two
The carbon linked to two alkyl /carbons and one
The carbon linked to three alkyl groups/carbons and no
These are indicated below:
(c)
Interpretation: Primary, secondary and tertiary hydrogen in below structure along with IUPAC name should be labeled.
Concept introduction: In accordance with IUPAC convention longest chain can be found from either direction provided it is longest and digits indicate the position of carbon or the position of branched alkyl chain in cases of branched hydrocarbons. All the side chains are named in alphabetical order.
The IUPAC system for nomenclature of straight hydrocarbon makes use of table given as follows:
Beside the IUPAC names there are certain common names. The common prefixes used include prefixes” iso-“ and “neo-“ .For example isobutane is common name used popularly for
The carbon linked to one alkyl / carbon while other two
The carbon linked to two alkyl /carbons and one
The carbon linked to three alkyl groups/carbons and no
These are indicated below:
(d)
Interpretation: Primary, secondary and tertiary hydrogen in below structure along with IUPAC name should be labeled.
Concept introduction: In accordance with IUPAC convention longest chain can be found from either direction provided it is longest and digits indicate the position of carbon or the position of branched alkyl chain in cases of branched hydrocarbons. All the side chains are named in alphabetical order.
The IUPAC system for nomenclature of straight hydrocarbon makes use of table given as follows:
Beside the IUPAC names there are certain common names. The common prefixes used include prefixes” iso-“ and “neo-“ .For example isobutane is common name used popularly for
The carbon linked to one alkyl / carbon while other two
The carbon linked to two alkyl /carbons and one
The carbon linked to three alkyl groups/carbons and no
These are indicated below:
(e)
Interpretation: Primary, secondary and tertiary hydrogen in below structure along with IUPAC name should be labeled.
Concept introduction: In accordance with IUPAC convention longest chain can be found from either direction provided it is longest and digits indicate the position of carbon or the position of branched alkyl chain in cases of branched hydrocarbons. All the side chains are named in alphabetical order.
The IUPAC system for nomenclature of straight hydrocarbon makes use of table given as follows:
Beside the IUPAC names there are certain common names. The common prefixes used include prefixes” iso-“ and “neo-“ .For example isobutane is common name used popularly for
The carbon linked to one alkyl / carbon while other two
The carbon linked to two alkyl /carbons and one
The carbon linked to three alkyl groups/carbons and no
These are indicated below:
(f)
Interpretation: Primary, secondary and tertiary hydrogen in below structure along with IUPAC name should be labeled.
Concept introduction: In accordance with IUPAC convention longest chain can be found from either direction provided it is longest and digits indicate the position of carbon or the position of branched alkyl chain in cases of branched hydrocarbons. All the side chains are named in alphabetical order.
The IUPAC system for nomenclature of straight hydrocarbon makes use of table given as follows:
Beside the IUPAC names there are certain common names. The common prefixes used include prefixes” iso-“ and “neo-“ .For example isobutane is common name used popularly for
The carbon linked to one alkyl / carbon while other two
The carbon linked to two alkyl /carbons and one
The carbon linked to three alkyl groups/carbons and no
These are indicated below:

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Chapter 2 Solutions
ORGANIC CHEMISTRY (LL)-PACKAGE
- I need help with the followingarrow_forwardFor Raman spectroscopy/imaging, which statement is not true regarding its disadvantages? a) Limited spatial resolution. b) Short integration time. c) A one-dimensional technique. d) Weak signal, only 1 in 108 incident photons is Raman scattered. e) Fluorescence interference.arrow_forwardUsing a cell of known pathlength b = 1.25115 x 10-3 cm, a water absorption spectrum was measured. The band at 1645 cm-1, assigned to the O-H bending, showed an absorbance, A, of 1.40. a) Assuming that water density is 1.00 g/mL, calculate the water molar concentration c (hint: M= mole/L) b) Calculate the molar absorptivity, a, of the 1645 cm-1 band c) The transmitted light, I, can be written as I= Ioexp(-xb), where x is the absorption coefficient (sometimes designated as alpha), Io is the input light, and b is the cell pathlength. Prove that x= (ln10)*x*c. (Please provide a full derivation of the equation for x from the equation for I). d) Calculate x for the 1645 cm-1 bandarrow_forward
- For CARS, which statement is not true regarding its advantages? a) Contrast signal based on vibrational characteristics, no need for fluorescent tagging. b) Stronger signals than spontaneous Raman. c) Suffers from fluorescence interference, because CARS signal is at high frequency. d) Faster, more efficient imaging for real-time analysis. e) Higher resolution than spontaneous Raman microscopy.arrow_forwardDraw the major product of the Claisen condensation reaction between two molecules of this ester. Ignore inorganic byproducts. Incorrect, 5 attempts remaining 1. NaOCH3/CH3OH 2. Acidic workup Select to Draw O Incorrect, 5 attempts remaining The total number of carbons in the parent chain is incorrect. Review the reaction conditions including starting materials and/or intermediate structures and recount the number of carbon atoms in the parent chain of your structure. OKarrow_forwardUsing a cell of known pathlength b = 1.25115 x 10-3 cm, a water absorption spectrum was measured. The band at 1645 cm-1, assigned to the O-H bending, showed an absorbance, A, of 1.40. a) Assuming that water density is 1.00 g/mL, calculate the water molar concentration c (hint: M= mole/L) b) Calculate the molar absorptivity, a, of the 1645 cm-1 band c) The transmitted light, I, can be written as I= Ioexp(-xb), where x is the absorption coefficient (sometimes designated as alpha), Io is the input light, and b is the cell pathlength. Prove that x= (ln10)*x*c d) Calculate x for the 1645 cm-1 bandarrow_forward
- Organic And Biological ChemistryChemistryISBN:9781305081079Author:STOKER, H. Stephen (howard Stephen)Publisher:Cengage Learning,General, Organic, and Biological ChemistryChemistryISBN:9781285853918Author:H. Stephen StokerPublisher:Cengage Learning

