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Q: Which is a stronger base: RO- or RS-?
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Q: Which compound is the strongest base?
A: ANSWERE IS DISCUSSED BELOW :
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Q: Which compound is the stronger base?
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A: Figure 1.
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Q: 2. Draw the mechanism (curved arrows) for each acid-base reaction b) d)
A: The given reactions are : Curved arrows mechanism of the given reactions are = ?
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A: Given : structure of molecules Basic strength is inversely proportional to percentage s character
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Q: Which is a stronger acid? Why?
A: The stronger acid is also identified by its resonance structures. More is the resonance stabilized…
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Q: Draw the major organic product of the Bronsted acid-base reaction. Include all lone pairs and…
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A: To find: Which is stronger acid?
Q: For given pair of compounds, identify which compound is the stronger base, and explain your choice:…
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A: This question belong to General organic chemistry Aromatic compounds. Aromatic compounds follow…
Q: (A) B) P3-or S3--
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Q: Rank the following in order of increasing basicity. The first compound in your list should be the…
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Q: Which compound is a stronger base?
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Q: Rank the nitrogens below in order of decreasing basicity (most basic to least basic) NH (c) (a) (b)…
A: The answer is given as follows Basicity order is c>a>b
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A:
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- please note its (s) (aq) or (l)Propoxide (CH3CH2CH2O- ) is a larger molecule than ethoxide (CH3CH2O- ), yet they are equally basic. Explain why they are equally basic.A) Which compounds in the picture provided has an acidic group B) Which compounds in the picture provided has a basic group? Thank You!
- Which is a stronger base: RO- or RS-?Amides are weak nucleophiles but their conjugate bases are string nucleophiles. The amide drawn below can be deprotonated in four possible locations, labeled A-D but two are considerably more acidic than the others. Draw the two different Bronsted Lowery acid/base reactions (using HO- as the BL base) showing the deprotonation at these two locations. Draw all RS with arrows for both conjugate bases but no hybrids. Based on your resonance analysis which location is the most acidic in the molecule? Why is it most acidic? Amides can also be protonated by a strong acid in two different locations. Draw two different conjugate acids for the amide above as well as RS with arrows for each. Based on your resonance analysis which atom is the most basic in an amide?Base catalysts speed up the nucleophilic reactions of carbonyl compounds. How? Explain.