(a)
Interpretation:
The constitutional isomer, which is formed greatest yield in the given reaction should be given.
Concept introduction:
Dehydration reaction:
Removal of water molecule from the reaction when the alcohol is treated with strong acid like sulfuric acid is known as dehydration reaction, for example
Alcohols are react with acids like hydrochloric acid or hydrobromic to yields the corresponding carbocation intermediates, this carbocation intermediate undergoes elimination reaction to give a corresponding
The stability of carbocation is given below,
Tertiary carbocation is more stable than the secondary and primary.
Cis–trans isomerism (or) geometric isomerism or configurational isomerism:
The
The functional groups are in opposite to each other in the carbon chain is called trans isomer.
Two similar functional groups are in same side which is called as Z-isomer.
Two similar functional groups are opposite side which is called as E-isomer.
Stereoisomers: same molecular formula and sequence of bonded atoms (constitution), but differ in the three-dimensional orientations of their atoms in space.
(b)
Interpretation:
The stereoisomer, which is formed greatest yield in the given reaction should be given.
Concept introduction:
Dehydration reaction:
Dehydration reaction:
Removal of water molecule from the reaction when the alcohol is treated with strong acid like sulfuric acid is known as dehydration reaction, for example
Alcohols are react with acids like hydrochloric acid or hydrobromic to yields the corresponding carbocation intermediates, this carbocation intermediate undergoes elimination reaction to give a corresponding alkene as a product.
The stability of carbocation is given below,
Tertiary carbocation is more stable than the secondary and primary.
Cis–trans isomerism (or) geometric isomerism or configurational isomerism:
The functional groups are in the same side of the carbon chain is called cis isomer.
The functional groups are in opposite to each other in the carbon chain is called trans- isomer.
Two similar functional groups are in same side which is called as Z-isomer.
Two similar functional groups are opposite side which is called as E-isomer.
Stereoisomers: same molecular formula and sequence of bonded atoms (constitution), but differ in the three-dimensional orientations of their atoms in space.
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Chapter 11 Solutions
EBK ORGANIC CHEMISTRY
- Identify the missing organic reactants in the following reaction: X + Y H+ two steps Note: This chemical equation only focuses on the important organic molecules in the reaction. Additional inorganic or small-molecule reactants or products (like H2O) are not shown. In the drawing area below, draw the skeletal ("line") structures of the missing organic reactants X and Y. You may draw the structures in any arrangement that you like, so long as they aren't touching. Click and drag to start drawing a structure. Х :arrow_forwardDraw the mechanism of friedel-crafts acylation using acetyl chloride of m-Xylenearrow_forwardI need help naming these in IUPACarrow_forward
- H R Part: 1/2 :CI: is a/an electrophile Part 2 of 2 Draw the skeletal structure of the product(s) for the Lewis acid-base reaction. Include lone pairs and formal charges (if applicable) on the structures. 4-7: H ö- H Skip Part Check X :C1: $ % L Fi Click and drag to start drawing a structure. MacBook Pro & ㅁ x G 0: P Add or increase positive formal cha Save For Later Submit ©2025 McGraw Hill LLC. All Rights Reserved. Terms of Use | Privacy Centearrow_forwardDraw the friedel-crafts acylation mechanism of m-Xylenearrow_forwardDon't used hand raiting and don't used Ai solutionarrow_forward
- 1. Base on this experimental results, how do you know that the product which you are turning in is methyl 3-nitrobenzoate(meta substituted product ) rather than either of the other two products? 2. What observation suggests that at least a small amount of one or both of the other two isomers are in the mother liquor?arrow_forwardExplain Huckel's rule.arrow_forwardhere is my question can u help me please!arrow_forward
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