When combined with alcohol some over the counter drugs can:
2 answers:
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Answer:
I attached the answer as an image. I also drew in the two most acidic hydrogens.
Explanation:
This goes through the 'benzyne' intermediate, meaning it does an E2-looking reaction by expelling a leaving group (chloride) from the adjacent part of the ring using the amide as a strong base. The triple-bonded benzyne has absurd bond angle strain, and is vulnerable to a good nucleophile like an amide ion, and the resultant sp2 anion is then reprotonated by the acid. I didn't draw in the acid-base reaction in step one, or the spectator ion (sodium).
Answer: 1. C. polar covalent: electrons shared between silicon and sulfur but attracted more to the sulfur
2. B)
3. B) Fluorine
Explanation:
1. A polar covalent bond is defined as the bond which is formed when there is a difference of electronegativities between the atoms.
Electronegativity difference = electronegativity of sulphur- electronegativity of silicon = 2.5 -1.8 = 0.7
Thus as electronegativity difference is less than 1.7 , the cond is polar covalent and as electronegativity of sulphur is more , the electrons will be more towards sulphur.
2. A molecular compound is usually composed of two or more nonmetal elements. Example:
Ionic compound is formed by the transfer of electrons from metals to non metals. Example: ,
and
3. For formation of a neutral ionic compound, the charges on cation and anion must be balanced. The cation is formed by loss of electrons by metals and anions are formed by gain of electrons by non metals.
Here K is having an oxidation state of +1 and as the compound formed is KZ, the oxidation state of non metallic element Z should be -1. Thus the element Z is flourine which exists as diatomic gas