
Concept explainers
Interpretation:
The hydrogen bonding possible between G-C base pair when both bases are in their enol form is to be drawn. Comparing this with the hydrogen bonding in the base pair shown in Figure 14-31 and Figure 14-33, which scenario maximizes hydrogen bonding is to be determined.
Concept introduction:
A hydrogen bond is a form of dipole-dipole interaction. It occurs between a hydrogen atom bonded to a highly electronegative atom like N, O, or F and an atom of one of these from another molecule. It is also possible for the two groups to be from the same molecule. H-bond is formed when the electronegative atom from one molecule/group donates its lone pair to the partially positively charged hydrogen-bonded to the electronegative atom.
Compounds containing an enol group – an OH bonded to a carbon double-bonded to another carbon – generally rearrange to the more stable keto form in a process known as tautomerization.

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Chapter 14 Solutions
Organic Chemistry: Principles And Mechanisms (second Edition)
- 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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