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(a)
Interpretation:
The product obtained in the reaction of 3-acetylfuran with nitric acid and sulfuric acid has to be given.
Concept Introduction:
The reaction of sulfuric acid and nitric acid results in the generation of nitronium ion which attacks the most nucleophilic position of the reactant. The nucleophilicity of the carbon atoms present in the furan depends upon the nature of substituents attached to it.
(b)
Interpretation: The product formed in the reaction of 2-nitrothiophene with bromine has to be given.
Concept Introduction:
The reaction of bromine with alkyl and aryl groups is a type of electrophilic substitution reaction in which
(c)
Interpretation: The product obtained in the reaction of 4-dimethylaminepyridine with methyl iodide has to be given.
Concept Introduction:
Tertiary
(d)
Interpretation: The product obtained in the reaction of pyridione with
Concept Introduction:
Phosphorus trichloride reacts with hydroxyl group and leads to the formation of
(e)
Interpretation: The product obtained in the reaction of 1,4-dimethylpyridine hydroxide with formic acid and hydrochloric acid has to be given.
Concept Introduction:
Tertiary amines exist as quaternary ammonium salts in the electrolytic solution. Quaternary ammonium salts are the salts of nitrogen in which four groups are attached to nitrogen and it exhibits a positive charge which is stabilized by the negative charges present in the solution.
(f)
Interpretation: The product obtained in the reaction of pyrrole with
Concept Introduction:
The alkyl group attached to magnesium bromide acts as a nucleophile because carbon atom is more electronegative as compared to magnesium due to which carbon atom exhibits partial negative charge in the reaction of Grignard reagent.
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Chapter 19 Solutions
Pearson eText Organic Chemistry -- Instant Access (Pearson+)
- can someone draw out the reaction mechanism for this reaction showing all bonds, intermediates and side products Comment on the general features of the 1H-NMR spectrum of isoamyl ester provided belowarrow_forwardWhat would be the best choices for the missing reagents 1 and 3 in this synthesis? 1. PPh3 3 2. n-BuLi • Draw the missing reagents in the drawing area below. You can draw them in any arrangement you like. • Do not draw the missing reagent 2. If you draw 1 correctly, we'll know what it is. • Note: if one of your reagents needs to contain a halogen, use bromine. Click and drag to start drawing a structure.arrow_forwardIdentify 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_forward
- I am struggling with the IUPAC (sys H Reply ☑Mark as Unreadarrow_forwardDon't used hand raiting and don't used Ai solution and correct answerarrow_forwardH 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_forward
- Draw the friedel-crafts acylation mechanism of m-Xylenearrow_forwardDon't used hand raiting and don't used Ai solutionarrow_forward1. 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_forward
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