(a)
Interpretation:
The systematic (IUPAC) name of each group substituent in the given organic molecules should be draw and identified.
Concept introduction:
The several organic compounds can be named by using certain rules given by IUPAC (International Union for Pure and applied chemistry).
The IUPAC name consists of three parts in major namely Prefix, suffix and root word.
Prefix: Represents the substituent present in the molecule and its position in the root name.
For example the saturated hydrocarbons not only from only carbon-hydrogen bonds rather than the carbon-carbon bonds that have added hydrogen atoms. These
Suffix: Denotes the presence of
Root word: It represents the longest continuous carbon skeleton of the organic molecule.
To identify: The systematic (stereo chemical) name for the given molecule (a).
(b)
Interpretation:
The systematic (IUPAC) name of each group substituent in the given organic molecules should be draw and identified.
Concept introduction:
The several organic compounds can be named by using certain rules given by IUPAC (International Union for Pure and applied chemistry).
The IUPAC name consists of three parts in major namely Prefix, suffix and root word.
Prefix: Represents the substituent present in the molecule and its position in the root name.
For example the saturated hydrocarbons not only from only carbon-hydrogen bonds rather than the carbon-carbon bonds that have added hydrogen atoms. These alkanes have to prefix ‘cyclo’ due to the configuration of rings of carbon atoms.
Suffix: Denotes the presence of functional group if any in the molecule. It can be an alkane, alkene, alkyne, alcohol, carboxylic acid, alcohol etc. For example alkene molecules, suffix will be ‘ene’. (Or) If the presence of completely saturated alkane molecules, suffix will be ‘ane’.
Root word: It represents the longest continuous carbon skeleton of the organic molecule.
To identify: The systematic (stereo chemical) name for the given molecule (a).
(c)
Interpretation:
The systematic (IUPAC) name of each group substituent in the given organic molecules should be draw and identified.
Concept introduction:
The several organic compounds can be named by using certain rules given by IUPAC (International Union for Pure and applied chemistry).
The IUPAC name consists of three parts in major namely Prefix, suffix and root word.
Prefix: Represents the substituent present in the molecule and its position in the root name.
For example the saturated hydrocarbons not only from only carbon-hydrogen bonds rather than the carbon-carbon bonds that have added hydrogen atoms. These alkanes have to prefix ‘cyclo’ due to the configuration of rings of carbon atoms.
Suffix: Denotes the presence of functional group if any in the molecule. It can be an alkane, alkene, alkyne, alcohol, carboxylic acid, alcohol etc. For example alkene molecules, suffix will be ‘ene’. (Or) If the presence of completely saturated alkane molecules, suffix will be ‘ane’.
Root word: It represents the longest continuous carbon skeleton of the organic molecule.
To identify: The systematic (stereo chemical) name for the given molecule (a).
(d)
Interpretation:
The systematic (IUPAC) name of each group substituent in the given organic molecules should be draw and identified.
Concept introduction:
The several organic compounds can be named by using certain rules given by IUPAC (International Union for Pure and applied chemistry).
The IUPAC name consists of three parts in major namely Prefix, suffix and root word.
Prefix: Represents the substituent present in the molecule and its position in the root name.
For example the saturated hydrocarbons not only from only carbon-hydrogen bonds rather than the carbon-carbon bonds that have added hydrogen atoms. These alkanes have to prefix ‘cyclo’ due to the configuration of rings of carbon atoms.
Suffix: Denotes the presence of functional group if any in the molecule. It can be an alkane, alkene, alkyne, alcohol, carboxylic acid, alcohol etc. For example alkene molecules, suffix will be ‘ene’. (Or) If the presence of completely saturated alkane molecules, suffix will be ‘ane’.
Root word: It represents the longest continuous carbon skeleton of the organic molecule.
To identify: The systematic (stereo chemical) name for the given molecule (a).

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Chapter 19 Solutions
ORGANIC CHEMISTRY WILEYPLUS ACCESS>I<
- What is the reaction mechanism for this?arrow_forwardWhat is the reaction mechanism for this?arrow_forwardCurved arrows are used to illustrate the flow of electrons. Using the provided starting and product structures, draw the curved electron-pushing arrows for the following reaction or mechanistic step(s). Be sure to account for all bond-breaking and bond-making steps. + Drawing Arrows CH3ONA, CH3OH heat : Br:O Na → H H Br Na + H H H H H :0: .H + Undo Reset Done Q CH3 Drag To Pan +arrow_forward
- What is the reaction mechanism for this?arrow_forward20.19 Predict the structure of the major 1,2-addition product formed by reaction of one mole of Cl₂ with 3-methylenecyclohexene. Also predict the structure of the 1,4-addition product formed under these conditions. 20.20 Which of the two molecules shown do you expect to be the major product formed by 1,2-addition of HCI to cyclopentadiene? Explain. Cyclopentadiene + HC 3-Chlorocyclopentene (racemic) or 4-Chlorocyclopentene (racemic)arrow_forward20.35 Propose structural formulas for compounds A and B and specify the configuration of compound B. EtO₂C 250°C C14H2004 CO₂Et 1. Oso, then NaHSO3 2. HIO4 C14H2006 A Barrow_forward
- 20.21 Predict the major product formed by 1,4-addition of HCI to cyclopentadiene. 20.22 Draw structural formulas for the two constitutional isomers with the molecular for- mula C₂H,Br, formed by adding one mole of Br, to cyclopentadiene.arrow_forwardAdd substituents to draw the conformer below (sighting down the indicated bond), then rotate the back carbon to provide the conformation that will be capable of an E2 elimination. R/S stereochemistry is graded. + I I H CH3 Ph Досн Br OCH 3 Drawing Q H Atoms, Bonds and Rings Charges Tap a node to see suggestions. H H H H H Undo Reset Remove Done Rotatearrow_forward20.17 Predict the structure of the major product formed by 1,2-addition of HBr to 3-methylenecyclohexene. 3-Methylenecyclohexene 20.18 Predict the major product formed by 1,4-addition of HBr to 3-methylenecyclohexene.arrow_forward
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