Answer : The correct answer for a) 4-bromo-2-iodo-4-methyl pentane and b)5-bromo-2-ethoxy-2-methyl pentane.
A) Reaction with NaI :
Reaction of alkyl halide with NaI is known as Finkelstein Reaction . The acetone is used as solvent . It involves bimolecular nucleophillic substitution rmechanism (SN²) . There is replecement of one halogen with other occurs .
The incoming Nucleophile(Nu⁻) (halide) attacks on carbon from back side , while the leaving group (halide) leaves the compound from front side , simultaneously. The product so formed have is inverted .(Image)
NaI releases I⁻ ion which act as nucelophile and attacks on C1 carbon and Br⁻ from C1 carbon is released . Out of two bromines at C1 and C4 carbons , C1 is primary carbon which is less sterically hindered while C-4 is tertiary carbon and sterically hindered . So it is easy for incoming Nu⁻ to attack on C1 carbon .So Br⁻ is repleaced by I⁻.
1,4-dibromo-4-methylpentane + NaI → 4-bromo-1-iodo-4-methylpentane
The product formed from reaction between 1,4-dibromo-4-methylpentane and NaI is 4-bromo-1-iodo-4-methylpentane . (Image)
B) Reaction with AgNO3 :
Reaction of alkyl halide with AgNO3 in ethanol takes place via SN¹ ( unimolecular nucleophilic substitution ) mechanism . In this leaving group(halide) leaves from alkyl halide forming an intermediate carbocation species . The incoming Nu⁻ attack on this carbocation.
AgNO3 reacts releases Ag⁺ion which abstract Br⁻ of C-4 carbon from 1,4-dibromo-4-methylpentane. THis forms tertiary carbocation which is more stable than carbocation formed by removal of Br from C-1 . The ethanol being more Nucleophilic than NO₃⁻ (from AgNO₃), attacks on this carbocation .(Image )
The product formed as a result is 5-bromo-2-ethoxy-2-methyl pentane.
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Explanation:
Answer:
0.0432M
Explanation:
We begin by writing a balanced equation for the reaction. This is illustrated below:
NaOH + HCl —> NaCl + H2O
From the equation above,
The number of mole of the acid (nA) = 1
The number of mole of the base (nB) = 1
Data obtained from the question include:
Vb (volume of the base) = 54mL
Cb (concentration of the base) = 0.1M
Va (volume of the acid) = 125mL
Ca ( concentration of the acid) =?
Using CaVa/CbVb = nA/nB, the concentration of the acid can easily be obtained as shown below:
CaVa/CbVb = nA/nB
Ca x 125 / 0.1 x 54 = 1
Cross multiply to express in linear form:
Ca x 125 = 0.1 x 54
Divide both side by 125
Ca = (0.1 x 54) / 125
Ca = 0.0432M
Therefore, the concentration of the acid is 0.0432M
<h3><u>Answer;</u></h3>
Empirical formula = C₂H₃O
Molecular formula = C₁₄H₂₁O₇
<h3><u>Explanation</u>;</h3>
Empirical formula
Moles of;
Carbon = 55.8 /12 = 4.65 moles
Hydrogen = 7.04/ 1 = 7.04 moles
Oxygen = 37.16/ 16 = 2.3225 moles
We then get the mole ratio;
4.65/2.3225 = 2.0
7.04/2.3225 = 3.0
2.3225/2.3225 = 1.0
Therefore;
The empirical formula = <u>C₂H₃O</u>
Molecular formula;
(C2H3O)n = 301.35 g
(12 ×2 + 3× 1 + 16×1)n = 301.35
43n = 301.35
n = 7
Therefore;
Molecular formula = (C2H3O)7
<u> = C₁₄H₂₁O₇</u>
Answer:
When C1 is labeled in glucose, it ends up in the methyl group of pyruvate.
Aldolase cleaves a hexose into two trioses.
[See the image attached].
Asterisk indicates the label.
When C1 is labeled in glucose, it ends up in the carboxyl group of pyruvate.