Interpretation:
The stereoisomer required to obtain the given products in presence of
Concept introduction:
Addition Reaction: It is defined as
In addition reaction of
Stereoisomers: Two compounds with same molecular formula but different in their orientation are considered as isomers.
The presence of atom with non-super impossible mirror image is defined as enantiomers which are given
Meso compound: The compound with chiral carbon that also have plane of symmetry which actually makes the compound achiral that does not have an enantiomer (Non-superimposable mirror images).
R and S nomenclature: it is used to assign the molecule using CIP rules.
The CIP rules are as follows:
Select the chiral carbon and assign the numbers according to the decreasing
If the numbering follows clockwise direction then the molecule is termed as R and if it follows anti-clockwise direction then molecule is termed as S.
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EBK ORGANIC CHEMISTRY
- A chemist allows some pure (2S,3R)-3-bromo-2,3-diphenylpentane to react with a solution of sodium ethoxide(NaOCH2CH3) in ethanol. The products are two alkenes: A (cis-trans mixture) and B, a single pure isomer. Under thesame conditions, the reaction of (2S,3S)-3-bromo-2,3-diphenylpentane gives two alkenes, A (cis-trans mixture) and C.Upon catalytic hydrogenation, all three of these alkenes (A, B, and C) give 2,3-diphenylpentane. Determine the structuresof A, B, and C; give equations for their formation; and explain the stereospecificity of these reactionsarrow_forwardFf.22. With explanation...arrow_forwardWrite a stepwise mechanism for each of the following reactions. Explain why a more stable alkyne (but-2-yne) is isomerized to a less stable alkyne (but-1-yne), but under similar conditions. 2.5-dimethylhex-3-yne forms 2,5-dimethylhexa-2.3-diene.arrow_forward
- Pick the reactant or solvent in each part that gives the faster elimination reaction.a. reaction of -OH with 1-chloro-1-methylcyclohexane or 1-chloro-3-methylcyclohexaneb. reaction of H2O with CH3CH(Cl)CH2CH3 or (CH3)2C(Cl)CH2CH3c. reaction of (CH3)3CCl with -OH in H2O or DMSOarrow_forwardDraw the structure(s) of the most favorable products for the following:arrow_forwardG.115. I need all three sub parts .....arrow_forward
- 7. The reaction of A) B) 2-methylheptane (R)-2-methyl-5-heptanol (S)-6-methyl-3-heptanol with H₂/Ni forms D) (R and S)-6-methyl-3-heptanol E) Achiral 6,6-dimethyl-3-hexanolarrow_forwardWhen the alkene A was treated first with Hg(OAc)2 in MeOH and second with NaBH4 the product was the ether B. Using curved arrows please give the mechanism for the first step of (Hg(OAc)2 in MeOH) this reaction, including any regioselectivity or stereoselectivity. H3C 1. Hg(OAc)2, MeOH H3C O-CH3 =CH2 ✓ -CH3 H3C 2. NaBH H3C A Barrow_forwardDraw a structural formula for the major organic product of the following reaction: CH2CI2 Br2 CH3CH=CHCH2CH(CH3)2 + Show product stereochemistry IF the reactant alkene has both carbons of the double bond within a ring. • Do not show stereochemistry in other cases. • If enantiomers are formed, just draw one. opy aste - [F ChemDoodlearrow_forward
- Draw a structural formula for the major organic product of the following reaction: CH3 CH3 ● CH3 CH3 AAVIL + Br₂ Show product stereochemistry IF the reactant alkene has both carbons of the double bond within a ring. • Do not show stereochemistry in other cases. ● If enantiomers are formed, just draw one. CH₂Cl₂ Sn [F ? ChemDoodleⓇarrow_forwardG.133.arrow_forwardKl117.arrow_forward
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