Answer:
Burning wood
Explanation:
the fire releases heat into the air from the burning wood
Answer:
10.6 g CO₂
Explanation:
You have not been given a limiting reagent. Therefore, to find the maximum amount of CO₂, you need to convert the masses of both reactants to CO₂. The smaller amount of CO₂ produced will be the accurate amount. This is because that amount is all the corresponding reactant can produce before it runs out.
To find the mass of CO₂, you need to (1) convert grams C₂H₂/O₂ to moles (via molar mass), then (2) convert moles C₂H₂/O₂ to moles CO₂ (via mole-to-mole ratio from reaction coefficients), and then (3) convert moles CO₂ to grams (via molar mass). *I had to guess the chemical reaction because the reaction coefficients are necessary in calculating the mass of CO₂.*
C₂H₂ + O₂ ----> 2 CO₂ + H₂
9.31 g C₂H₂ 1 mole 2 moles CO₂ 44.0095 g
------------------ x ------------------- x ---------------------- x ------------------- =
26.0373 g 1 mole C₂H₂ 1 mole
= 31.5 g CO₂
3.8 g O₂ 1 mole 2 moles CO₂ 44.0095 g
------------- x -------------------- x ---------------------- x -------------------- =
31.9988 g 1 mole O₂ 1 mole
= 10.6 g CO₂
10.6 g CO₂ is the maximum amount of CO₂ that can be produced. In other words, the entire 3.8 g O₂ will be used up in the reaction before all of the 9.31 g C₂H₂ will be used.
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.
Answer:any substance which may be harmful to the environment or hazardous to your health if inhaled, ingested or absorbed through the skin.
Explanation: