(a)
Interpretation:
The stereoisomers of the given compound has to be drawn.
Concept introduction:
Stereoisomers are isomers which have different spatial arrangement in spite of same bond connectivity. Stereoisomers are due to the presence of stereocenter. Stereocenter may be an atom axis (bond) or plane from which interchanging of two groups leads to stereoisomers.
Asymmetric center is a stereocenter which arises to hydrocarbons if the carbon is bonded to four different groups.
The equation for finding Stereoisomers from number of asymmetric centers in compounds is
(b)
Interpretation:
The stereoisomers of the given compound has to be drawn.
Concept introduction:
Stereoisomers are isomers which have different spatial arrangement in spite of same bond connectivity. Stereoisomers are due to the presence of stereocenter. Stereocenter may be an atom axis (bond) or plane from which interchanging of two groups leads to stereoisomers.
Asymmetric center is a stereocenter which arises to hydrocarbons if the carbon is bonded to four different groups.
The equation for finding Stereoisomers from number of asymmetric centers in compounds is
(c)
Interpretation:
The stereoisomers of the given compound has to be drawn.
Concept introduction:
Stereoisomers are isomers which have different spatial arrangement in spite of same bond connectivity. Stereoisomers are due to the presence of stereocenter. Stereocenter may be an atom axis (bond) or plane from which interchanging of two groups leads to stereoisomers.
Asymmetric center is a stereocenter which arises to hydrocarbons if the carbon is bonded to four different groups.
The equation for finding Stereoisomers from number of asymmetric centers in compounds is
(d)
Interpretation:
The stereoisomers of the given compound has to be drawn.
Concept introduction:
Stereoisomers are isomers which have different spatial arrangement in spite of same bond connectivity. Stereoisomers are due to the presence of stereocenter.
Stereoisomers are isomers which have different spatial arrangement in spite of same bond connectivity. Stereoisomers are due to the presence of stereocenter. Stereocenter may be an atom axis (bond) or plane from which interchanging of two groups leads to stereoisomers.
Asymmetric center is a stereocenter which arises to hydrocarbons if the carbon is bonded to four different groups.
The equation for finding Stereoisomers from number of asymmetric centers in compounds is
(e)
Interpretation:
The stereoisomers of the given compound has to be drawn.
Concept introduction:
Stereoisomers are isomers which have different spatial arrangement in spite of same bond connectivity. Stereoisomers are due to the presence of stereocenter. Stereocenter may be an atom axis (bond) or plane from which interchanging of two groups leads to stereoisomers.
Asymmetric center is a stereocenter which arises to hydrocarbons if the carbon is bonded to four different groups.
The equation for finding Stereoisomers from number of asymmetric centers in compounds is
(f)
Interpretation:
The stereoisomers of the given compound has to be drawn.
Concept introduction:
Stereoisomers are isomers which have different spatial arrangement in spite of same bond connectivity. Stereoisomers are due to the presence of stereocenter. Stereocenter may be an atom axis (bond) or plane from which interchanging of two groups leads to stereoisomers.
Asymmetric center is a stereocenter which arises to hydrocarbons if the carbon is bonded to four different groups.
The equation for finding Stereoisomers from number of asymmetric centers in compounds is
(g)
Interpretation:
The stereoisomers of the given compound has to be drawn.
Concept introduction:
Stereoisomers are isomers which have different spatial arrangement in spite of same bond connectivity. Stereoisomers are due to the presence of stereocenter. Stereocenter may be an atom axis (bond) or plane from which interchanging of two groups leads to stereoisomers.
Asymmetric center is a stereocenter which arises to hydrocarbons if the carbon is bonded to four different groups.
The equation for finding Stereoisomers from number of asymmetric centers in compounds is
(h)
Interpretation:
The stereoisomers of the given compound has to be drawn.
Concept introduction:
Stereoisomers are isomers which have different spatial arrangement in spite of same bond connectivity. Stereoisomers are due to the presence of stereocenter. Stereocenter may be an atom axis (bond) or plane from which interchanging of two groups leads to stereoisomers.
Asymmetric center is a stereocenter which arises to hydrocarbons if the carbon is bonded to four different groups.
The equation for finding Stereoisomers from number of asymmetric centers in compounds is
(i)
Interpretation:
The stereoisomers of the given compound has to be drawn.
Concept introduction:
Stereoisomers are isomers which have different spatial arrangement in spite of same bond connectivity. Stereoisomers are due to the presence of stereocenter. Stereocenter may be an atom axis (bond) or plane from which interchanging of two groups leads to stereoisomers.
Asymmetric center is a stereocenter which arises to hydrocarbons if the carbon is bonded to four different groups.
The equation for finding Stereoisomers from number of asymmetric centers in compounds is
(j)
Interpretation:
The stereoisomers of the given compound has to be drawn.
Concept introduction:
Stereoisomers are isomers which have different spatial arrangement in spite of same bond connectivity. Stereoisomers are due to the presence of stereocenter. Stereocenter may be an atom axis (bond) or plane from which interchanging of two groups leads to stereoisomers.
Asymmetric center is a stereocenter which arises to hydrocarbons if the carbon is bonded to four different groups.
The equation for finding Stereoisomers from number of asymmetric centers in compounds is
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EBK ORGANIC CHEMISTRY
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- What is the preferred IUPAC name of the alkene shown in Figure below? CH3 CH3 CH3 `CH-CH3 A. 1-ethyl-2,4,5-trimethylcyclohexene B. 2-ethyl-1,4,5-trimethylcyclohexene C. 2-ethyl-1,4,5-trimethylcyclohex-1-ene D. 4-ethyl-1,2,5-trimethylcyclohexenearrow_forward3. Draw the structure of the following alkenes. Some of these compounds can show isomerism, and some cannot. Indicate which among these can show cis and trans isomers. a. hex-3-ene b. buta-1,3-diene c. 2,3-dimethylpent-2-ene 4. Draw the structure of the following alkenes. Some of these compounds can show isomerism, and some cannot. Indicate which among these can show cis and trans isomers. a. 3-ethylhexa-2,4-diene b. pent-1,3-diene c. 3,7-dichloroocta-2,5-dienearrow_forwardClassify each of the following hydrocarbons as saturated or unsaturated. Ethylcyclopentane Ethylcyclopentene 1,3-butadiene 2-methyl-2-pentene 2-methylcyclopentene 1,2-cyclopentadiene 2,3-dimethylpentanearrow_forward
- II. Give the condensed structural formula of each of the following ethers. 1. Isopropyl propyl ether 2. Methyl phenyl ether 3. 3-Methoxyhехane 4. 3-Methyl-2-isopropoxypentane 5. Ethoxycyclobutanearrow_forwardII. Draw the structural formula of the following: 1. 2,4-Diethyl-2-pentene 2. 4,5-Dibromo-2-hexene 3. 1,2-Dichlorocyclohexene 11. 1,2-Dichlorobutene 12. 1,3-Dichlorocyclobutene 13. 1,4-Cyclohexadiene 14. 2-Ethyl-1,4-octadiene 15. 4-Propyl-2-heptene 16. 2,3-Cyclohexadiene 17. 3-Ethylpropene 18. 1,7-Octadiene 19. 2,2,3-Trimethylheptene 20. Cyclooctene 4. Cis-3-octene 5. Trans-2-hexene 6. 3,5-Dimethyl-4-hexene 7. 2-Methyl-2-butene 8. 2,6-Dimethylheptene 9. 1-Butene 10. 2-Hexenearrow_forwardDetermine whether cis-trans isomerism is probable for the following cycloalkanes. If it is possible, draw structural formulas for the cis and trans isomers. a. 1-ethyl-1-methylcyclopentane b. ethylcyclohexane c. 1,4-diethylcyclohexane d. 1,1-dimethylcyclooctane e. methylcycloheptanearrow_forward
- Helparrow_forward1. What is the IUPAC name of the compound below? (Please refer to the image attached.) A. 2,2,5-pentylcyclohexane B. 1-Cyclohexyl-2,2,5-trimethylhexane C. 1-Cyclohexyl-1,1,4-trimethylpentane D. 2-Cyclohexyl-2,5-dimethylhexane E. None of the choices 2. The –ene ending suffix of alkene indicates that there is a presence of carbon-carbon _______ bonds in the organic compound. A. Single B. Double C. Triple D. Quadruple 3. It is an acyclic unsaturated hydrocarbon that contains one or more carbon–carbon triple bonds: A. Alkene B. Cycloalkene C. Alkyne D. Cycloalkynearrow_forwardWhat is the correct name for the following compound according to rules established by the International Union of Pure and Applied chemistry? (Disregard cis-trans isomerism) Select one: Br A. 1-bromo-2-propylcyclopentane O B. 1-(1-methylethyl)-2-bromocyclohexane O C. 2-(2-bromocyclohexyl)propane O D. 1-bromo-2-isopropylcyclohexanearrow_forward
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