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Answer:
The empirical formula = molecular formula = C13H18O2
Explanation:
in 100% compound we have 75.6 % Carbon ( Molar mass = 12g/mole), 8.80% hydrogen ( Molar mass = 1.01 g/mole) and 15.5% Oxygen (Molar mass = 16.01 g/mole).
Carbon: 75.6g / 12 = 6.29
Hydrogen: 8.80/ 1 = 8.80
Oxygen: 15.5/ 16 = 0.97
⇒0.97 is the smallest so we divide everything through by 0.97
C: 6.29 / 0.97 = 6.48 ≈ 6.5
H: 8.80 /0.97 = 9
O: 0.97 / 0.97 = 1
To get rid of decimals, we multiply by 2
C: 6.5 x 2 = 13
H: 9 x 2 = 18
O: 1 x 2 = 2
The empirical formula = C13H18O2
13x 12g/mol + 18x1g/mol + 2x 16g/mol = 156 + 18 + 32 = 206g/mol which is the molar mass of ibuprofen
The empirical formula = molecular formula = C13H18O2
Answer:
The correct answer is - option C.
Explanation:
Given: the melting point of HCl is
-114.8 °C, which suggests that below this temperature HCl will be solid.
and, since the boiling point of HCl is - 85.1 °C. It is also suggested that above this temperature HCl will be gas, Therefore.
Solid -114.8 - Ordered arrangement
Liquid -85.1c - Less orderly arranged
Gaseous - Least orderly arranged
Thus, at —90 °C, HCl will be present 'in the liquid state, At — 1 °C, HCl will be present in the gaseous state and at -129 °C, HCl will be present in the solid-state. So, the molecules will be organized in a more orderly manner
.
Thus, the correct answer is - option C
Answer: Step 1, Isomerase.
Explanation:
Form the version of palmitic acid in the step one by changing the double bond within alpha and beta carbon by Isomerase.
B and C are Isomers, the molecule only differ in configuration.
The first step in the reaction is the double bond of the Alkene going after the H of HBr. This protonates the Alkene via Markovnikov's rule, and forms a carbocation. The stability of this carbocation dictates the rate of the reaction.
<span>So to solve your problem, protonate all your Alkenes following Markovnikov's rule, and then compare the relative stability of your resulting carbocations. Tertiary is more stable than secondary, so an Alkene that produces a tertiary carbocation reacts faster than an Alkene that produces a secondary carbocation.
I hope my answer has come to your help. Thank you for posting your question here in Brainly. We hope to answer more of your questions and inquiries soon. Have a nice day ahead!
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