
Interpretation: It’s should be identified for the following compounds are not chiral one.
Concept introduction:
Structural Isomers are the structure of a molecule with same molecular formula but have different arrangements of bonds and atoms. For a single molecular formula of
A chiral carbon is the carbon atom which is substituted to four different groups. Due to presence of chiral carbon a molecule become chiral and it gives optical isomers also that is
All the substituents are different hence is is a chiral carbon and so molecule.
(1) Geometrical Isomerism: This type of isomerism in case of alkenes is known as cis-trans isomerism. When two same group or have similar priority present opposite side of double bond then isomer is known as trans isomer, and if both are present same side of the double bond then isomer is called as cis isomer.
(2) Structural Isomerism: Structural Isomers are the structure of a molecule with same molecular formula but have different arrangements of bonds and atoms and position of double bond also changes from more substituted to less substituted or vice-versa.

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Chapter 23 Solutions
Bundle: Chemistry & Chemical Reactivity, Loose-Leaf Version, 9th + OWLv2, 4 terms (24 Months) Printed Access Card
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- Part I. Draw reaction mechanism for the transformations of benzophenone to benzopinacol to benzopinaco lone and answer the ff: Pinacol (2,3-dimethyl, 1-3-butanediol) on treatment w/ acid gives a mixture of pina colone and (3,3-dimethyl-2-butanone) 2,3-dimethyl-1,3-butadiene. Give reasonable mechanism the formation of the products Forarrow_forwardShow the mechanism for these reactionsarrow_forwardDraw the stepwise mechanismarrow_forward
- Draw a structural formula of the principal product formed when benzonitrile is treated with each reagent. (a) H₂O (one equivalent), H₂SO₄, heat (b) H₂O (excess), H₂SO₄, heat (c) NaOH, H₂O, heat (d) LiAlH4, then H₂Oarrow_forwardDraw the stepwise mechanism for the reactionsarrow_forwardDraw stepwise mechanismarrow_forward
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