Answer:
32.1 g
Explanation:
Step 1: Write the balanced combustion reaction
C₄H₁₀ + 6.5 O₂ ⇒ 4 CO₂ + 5 H₂O
Step 2: Calculate the moles corresponding to 97.4 g of CO₂
The molar mass of CO₂ is 44.01 g/mol.
97.4 g × 1 mol/44.01 g = 2.21 mol
Step 3: Calculate the moles of butane that produced 2.21 moles of carbon dioxide
The molar ratio of C₄H₁₀ to CO₂ is 1:4. The moles of C₄H₁₀ required are 1/4 × 2.21 mol = 0.553 mol
Step 4: Calculate the mass corresponding to 0.553 moles of C₄H₁₀
The molar mass of C₄H₁₀ is 58.12 g/mol.
0.553 mol × 58.12 g/mol = 32.1 g
Answer:
32÷5
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goodluck tho❤
In a mechanical cycle, mechanical energy (mostly the the rotation) is used to get the desired result. The form of energy remains the same.
<span>In a thermodynamic cycle heat is converted to mechanical energy. That is to say there is conversion of energy.</span>
Answer:
The given isotope is Br 80
If 35 protons present then its atomic number is 35
Mass number is 80 so its meutrons are 45 because proton+ neutron = mass number
Its electron are 36 because of negative one charge
Explanation:
This reaction would give rise to two products.
- 2-bromo-3-methylhexane, and
- 3-bromo-3-methylhexane.
However, 2-bromo-3-methylhexane would be more common than 3-bromo-3-methylhexane among the products.
The hydrogen atom in a hydrogen bromide molecule carries a partial positive charge. It is attracted to the double bond region with a high electron density. The hydrogen-bromine bond breaks when HBr gets too close to a double bond to produces a proton
and a bromide ion
.
The proton would attack the double bond to produce a carbocation. It could attach itself to either the second or the third carbon atom.
Carbocations are unstable and might decompose over time. The first carbocation is more stable than the second for having three alkyl groups- i.e., straight carbon chains- attached to the center of the positive charge. Alkyl groups have stabilizing positive induction effect on positively-charged carbon. The second carbocation has only two, and is therefore not as stable. The first carbocation thus has the greatest chance to react with a bromide ion to produce a stable halocarbon.
Bromide ions are negatively charged. They attach themselves to carbocations at the center of positive charge. Adding a bromide ion to the first carbocation would produce 3-bromo-3-methylhexane whereas adding to the second produces 2-bromo-3-methylhexane.
The <em>most likely</em> product of this reaction is therefore 3-bromo-3-methylhexane.