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If you're asking about an ALKENE ( a carbon chain with a double bond) a TRANS (E) Isomer of 9-tricosENE (23 carbons) would be a straight chain with a double bond between carbon #9 and 10.
The CIS (Z) configuration would have the molecule bent to form a "U" with the bootom of the U being the 9 to 10 double bond. This makes the high priority carbons end up of the same (cis) side of the double bond.
What else can I help you with?
Which isomer packs more efficiently in the solid phase Cis isomer or Trans Isomer?
Trans isomer packs more efficiently in the solid phase compared to cis isomer. This is because trans isomers have a linear structure that allows them to stack more closely together, leading to stronger intermolecular interactions and more efficient packing.
Why the trans-benzalacetophenone isomer is major product in aldol condensation?
The trans-benzalacetophenone isomer is the major product in aldol condensation because it is more thermodynamically stable due to the extended conjugation in the molecule, leading to a more favorable resonance stabilization. The trans isomer also experiences less steric hindrance compared to the cis isomer, making it the preferred product.
Why trans is more stable than cis?
Because , Cis isomer are same group on same side of the c=c bond . & those are bulky group on the same side , they are formed steric repulsion to each other then Cis isomer are less stable than trans isomer is same group of opposite side of c=c bond no formation of steric repulsion to each other. and trans isomer is more stable than Cis isomer.....
Does 3-hexene have cis and trans isomers?
Yes, 3-hexene can exist as cis-3-hexene and trans-3-hexene isomers. In the cis isomer, the two alkyl groups are on the same side of the double bond, while in the trans isomer, they are on opposite sides.
What is the Chemical equation of Preparation of trans isomer of potassium dioxalatodiaquachromate 3?
The trans isomer of potassium dioxalatodiaquachromate (III) is prepared by treating the cis isomer with ammonia gas in a concentrated ammonia solution. The chemical equation for the preparation is: Cr(C2O4)(H2O)2(NH3)2 + NH3 → Cr(C2O4)(H2O)2(NH3) + H2O + NH4NO3
Which isomer packs more efficiently in the solid phase Cis isomer or Trans Isomer?
Trans isomer packs more efficiently in the solid phase compared to cis isomer. This is because trans isomers have a linear structure that allows them to stack more closely together, leading to stronger intermolecular interactions and more efficient packing.
Why the trans-benzalacetophenone isomer is major product in aldol condensation?
The trans-benzalacetophenone isomer is the major product in aldol condensation because it is more thermodynamically stable due to the extended conjugation in the molecule, leading to a more favorable resonance stabilization. The trans isomer also experiences less steric hindrance compared to the cis isomer, making it the preferred product.
Does 3 octene show cis trans isomerism?
Yes, 3-octene can exhibit cis-trans isomerism. In the cis isomer, the two methyl groups are on the same side of the double bond, while in the trans isomer, they are on opposite sides.
Why trans is more stable than cis?
Because , Cis isomer are same group on same side of the c=c bond . & those are bulky group on the same side , they are formed steric repulsion to each other then Cis isomer are less stable than trans isomer is same group of opposite side of c=c bond no formation of steric repulsion to each other. and trans isomer is more stable than Cis isomer.....
Does 3-hexene have cis and trans isomers?
Yes, 3-hexene can exist as cis-3-hexene and trans-3-hexene isomers. In the cis isomer, the two alkyl groups are on the same side of the double bond, while in the trans isomer, they are on opposite sides.
Draw the two geometrical isomers of chloroaquotetrammine cobalt 2 chloride?
Chloroaquotetrammine cobalt(II) chloride has two geometrical isomers: cis isomer and trans isomer. In the cis isomer, the chloride and ammonia ligands are adjacent to each other, while in the trans isomer, they are opposite to each other. This results in different spatial arrangements of ligands around the central cobalt ion.
What is the Chemical equation of Preparation of trans isomer of potassium dioxalatodiaquachromate 3?
The trans isomer of potassium dioxalatodiaquachromate (III) is prepared by treating the cis isomer with ammonia gas in a concentrated ammonia solution. The chemical equation for the preparation is: Cr(C2O4)(H2O)2(NH3)2 + NH3 → Cr(C2O4)(H2O)2(NH3) + H2O + NH4NO3
What formula represents trans isomer?
The general formula for a trans isomer is (E)-X-Y, where X and Y represent different groups attached to the double bond in a non-cyclic structure. The "E" notation indicates that the substituents are on opposite sides of the double bond.
What is an arrangement in which substituted groups are on the same side of a double bond?
A stereoisomer in which substituted groups are on the same side of a double bond is called a cis isomer. This arrangement results in a geometrical isomer with different chemical and physical properties compared to its trans isomer counterpart.
What is more polar either cis or trans?
cis. In cis, the electronegativity is concentrated on one side of the isomer, resulting in a net dipole moment, hence it is polar. In trans, the electronegativity is cancelled out by substituent groups on opposite sides of the isomer, there is no net dipole moment, and thus, it is non polar.
What is the difference between cis- and trans- isomers?
In cis-isomers, the carbon bonds are on the same side, and in the trans-isomers, the carbons are on the opposite side. Or put another way... In cis-isomers, the substituents bound to the C=C are on the same side, and the trans-isomer, the substituents bound to the C=C are on opposite sides.
If 4-tert-butylcyclohexanone were reduced with sodium borohydride which isomer of the product 4-tert-butylcyclohexan-1-ol would you expect to predominate?
The reduction of 4-tert-butylcyclohexanone with sodium borohydride would predominantly form the 4-tert-butylcyclohexan-1-ol isomer. This is due to the bulky tert-butyl group favoring the axial position in the chair conformation of the cyclohexane ring, leading to the 1-substituted alcohol as the major product.
