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Hint: Isomers are the compounds having the same molecular formula but different structural formula. The E and Z isomerism is the characteristic property of the unsaturated compounds that contain carbon – carbon double bonds as C=C. Z means together while the E prefix means opposite, so the arrangement of atoms is according to E, Z positions.
Complete answer:
Isomers are compounds having the same molecular formula but different structural formulas. Stereoisomerism is the property of isomers to exist in space. Stereo isomers have different spatial arrangement of the atoms between the same carbon bonds. E and Z isomers describe the stereo aspects of the carbons attached with double bonds.
The E isomer consists of the substituted groups on the opposite sides of the double bond, while in Z isomer, the substituted groups are on the same side of the double bonds.
We have been given pent-2-ene that has a formula$C{{H}_{3}}CH=CHC{{H}_{2}}C{{H}_{3}}$, which has a methyl and ethyl as substituted besides the carbon – carbon double bonds.
So, the E isomer where the carbon atoms of the substitutions are on the opposite sides is:
While, the Z isomer where the carbon atoms of the substitutions are on the same sides is:
Hence, E and Z isomers are pent-2-ene are as above, with substituted methyl and ethyl groups on opposite and same sides of double bonds respectively.
Note:
Unlike that of the cis and trans geometrical isomerism, E and Z isomerism can have same atoms attached as substituted groups and then also they can be identified as E and Z according to the priority of the atoms substituted. The higher priority atoms are of opposite sides (E) and the lower priority on the same side (Z). Atoms with high atomic numbers are given higher priority.
Complete answer:
Isomers are compounds having the same molecular formula but different structural formulas. Stereoisomerism is the property of isomers to exist in space. Stereo isomers have different spatial arrangement of the atoms between the same carbon bonds. E and Z isomers describe the stereo aspects of the carbons attached with double bonds.
The E isomer consists of the substituted groups on the opposite sides of the double bond, while in Z isomer, the substituted groups are on the same side of the double bonds.
We have been given pent-2-ene that has a formula$C{{H}_{3}}CH=CHC{{H}_{2}}C{{H}_{3}}$, which has a methyl and ethyl as substituted besides the carbon – carbon double bonds.
So, the E isomer where the carbon atoms of the substitutions are on the opposite sides is:
While, the Z isomer where the carbon atoms of the substitutions are on the same sides is:
Hence, E and Z isomers are pent-2-ene are as above, with substituted methyl and ethyl groups on opposite and same sides of double bonds respectively.
Note:
Unlike that of the cis and trans geometrical isomerism, E and Z isomerism can have same atoms attached as substituted groups and then also they can be identified as E and Z according to the priority of the atoms substituted. The higher priority atoms are of opposite sides (E) and the lower priority on the same side (Z). Atoms with high atomic numbers are given higher priority.
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