Martije has made a slight error in naming a compound monocarbon tetrabromide. What compound is she most likely naming, and what
2 answers:
The slight error has been to use the prefix mono to name monocarbon.
The compound she is most likely naming is:
.
As you see, the chemical formula has 1 atom of C, which is likely why she named it mono, and 4 atoms of Br.
The right name is carbon monobromide, i.e. you have to supress the prefix mono, as per IUPAC rules.
The compound she is most likely naming is:
As you see, the chemical formula has 1 atom of C, which is likely why she named it mono, and 4 atoms of Br.
The right name is carbon monobromide, i.e. you have to supress the prefix mono, as per IUPAC rules.
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So let's use some equations to represent the data [let R= cost of ring & B= cost of bracelet]
R= B + $ 36 .... (1)
B=
× R ... (2)
By using simultaneous equations to solve for B and R.
Substitute eq. (1) into eq. (2)
B = × (B + $36)
B =B + 
⇒ B = $48
By substituting value of B into ea (1)
If R = B + $36
R = ($48) + $36
= $84
∴ <span> the total of the two items = R + B
= $84 + $48
</span> = $132
R= B + $ 36 .... (1)
B=
By using simultaneous equations to solve for B and R.
Substitute eq. (1) into eq. (2)
B =
B =
⇒ B = $48
By substituting value of B into ea (1)
If R = B + $36
R = ($48) + $36
= $84
∴ <span> the total of the two items = R + B
= $84 + $48
</span> = $132
Answer:
No net change in reaction occurs in this nucleophilic acyl subtitution reaction
Explanation:
Sodium ethoxide in ethanol gives nucleophilic acyl substitution reaction with ethyl-2-methylpropanoate.
Here ethoxide group replaces an ethoxide group from ester through addition-ellimination pathway.
So, ultimately, the product of this reaction is identical with reactant i.e. ethyl-2-methylpropanoate is reproduced.
Hence one might observe no change during reaction as product and reactant of this reaction are same.
Mechanistic pathway has been shown below.
