
(a)
Interpretation:
The acceptable name for the following amide should be determined:
Concept Introduction:
An organic compound in which carboxy
The reaction which results in the formation of amide along with water on heating acids with
So, in order to give the IUPAC name to the amides, the rules for naming carboxylic acid is followed and -oic acid of the carboxylic acid is replaced by amide.
In order to give the name to the amide group, the following steps are followed:
- The parent (longest)
alkane chain is named as for carboxylic acids. - The -oic acid in the name is changed to -amide.
- The numbering of the chain is done in such a way that amide group and substituents gets the smaller number.
- N-alkyl is used to show each alkyl group bonded to -N atom in the name for secondary and tertiary amides.
For number of carbons atoms chain, the prefix is given as:
Carbon-1 meth
Carbon-2 eth
Carbon-3 prop
Carbon-4 but
Carbon-5 pent
Carbon-6 hex
Carbon-7 hept
Carbon-8 oct
Carbon-9 non
Carbon-10 dec
In order to write the common name of the amides, the common of acids are written from which the amide has been formed by replacing -oic acid in name from -amide.
(b)
Interpretation:
The acceptable name for the following amide should be determined:
Concept Introduction:
An organic compound in which carboxy functional group that is -COOH is bonded to the carbon atom is said to be a carboxylic acid. The general formula for carboxylic acid is RCOOH or RCO2H. When -OH (hydroxyl group) of the carboxylic acid is replaced by nitrogen (-N) then it results in the formation of an amide.
The reaction which results in the formation of amide along with water on heating acids with amine or ammonia is said to be amidation.
So, in order to give the IUPAC name to the amides, the rules for naming carboxylic acid is followed and -oic acid of the carboxylic acid is replaced by amide.
In order to give the name to the amide group, the following steps are followed:
- The parent (longest) alkane chain is named as for carboxylic acids.
- The -oic acid in the name is changed to -amide.
- The numbering of the chain is done in such a way that amide group and substituents gets the smaller number.
- N-alkyl is used to show each alkyl group bonded to -N atom in the name for secondary and tertiary amides.
For number of carbons atoms chain, the prefix is given as:
Carbon-1 meth
Carbon-2 eth
Carbon-3 prop
Carbon-4 but
Carbon-5 pent
Carbon-6 hex
Carbon-7 hept
Carbon-8 oct
Carbon-9 non
Carbon-10 dec
In order to write the common name of the amides, the common of acids are written from which the amide has been formed by replacing -oic acid in name from -amide.

Want to see the full answer?
Check out a sample textbook solution
Chapter 17 Solutions
General, Organic, and Biological Chemistry - 4th edition
- For 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_forwardI need help with the follloaingarrow_forward
- For a CARS experiment on a Raman band 918 cm-1, if omega1= 1280 nm, calculate the omega2 in wavelength (nm) and the CARS output in wavelength (nm).arrow_forwardI need help with the following questionarrow_forwardFor 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_forward
- Draw 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_forwardConvert 1.38 eV into wavelength (nm) and wavenumber (cm-1) (c = 2.998 x 108 m/s; h = 6.626 x 10-34 J*s).arrow_forward
- Organic Chemistry: A Guided InquiryChemistryISBN:9780618974122Author:Andrei StraumanisPublisher:Cengage LearningChemistry for Today: General, Organic, and Bioche...ChemistryISBN:9781305960060Author:Spencer L. Seager, Michael R. Slabaugh, Maren S. HansenPublisher:Cengage Learning

