The formation of Fossil Fuels.
The fossil fuels such as oil originate mostly from aquatic organism and are extracted on oil rigs located in oceans and seas. Most of the oil is procured this way.
Answer:
Scientists seek to eliminate all forms of bias from their research. However, all scientists also make assumptions of a non-empirical nature about topics such as causality, determinism and reductionism when conducting research. Here, we argue that since these 'philosophical biases' cannot be avoided, they need to be debated critically by scientists and philosophers of science.
Explanation:
Scientists are keen to avoid bias of any kind because they threaten scientific ideals such as objectivity, transparency and rationality. The scientific community has made substantial efforts to detect, explicate and critically examine different types of biases (Sackett, 1979; Ioannidis, 2005; Ioannidis, 2018; Macleod et al., 2015). One example of this is the catalogue of all the biases that affect medical evidence compiled by the Centre for Evidence Based Medicine at Oxford University (catalogueofbias.org). Such awareness is commonly seen as a crucial step towards making science objective, transparent and free from bias.
The name of this alkane is with central carbons are bonded to c h 3 is 2-methylbutane.
<h3>
What is alkane?</h3>
Alkanes belong to the family of saturated hydrocarbons with carbon carbon single bond.
For the given alkane;
CH₃ H
CH₃ - C - C - CH₃
H H
Thus, the name of this alkane is with central carbons are bonded to c h 3 is 2-methylbutane.
Learn more about alkane here: brainly.com/question/24270289
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Answer:
2-ethoxy-2-methylpropan-1-ol
Explanation:
On this reaction, we have an "<u>epoxide"</u> (2-methyl-1,2-epoxypropane). Additionally, we have <u>acid medium</u> (due to the sulfuric acid
). The acid medium will produce the <u>hydronium ion</u> (
). This ion would be attacked by the oxygen of the epoxide. Then a <u>carbocation</u> would be produced, in this case, the most stable carbocation is the <u>tertiary one</u>. Then an <u>ethanol</u> molecule acts as a nucleophile and will attack the carbocation. Finally, a <u>deprotonation </u>step takes place to produce <u>2-ethoxy-2-methylpropan-1-ol</u>.
See figure 1
I hope it helps!
The HCl added = 1.25 moles
and the moles of Na2HPO4 = 1 mole
Now when acid is added in the given solution of Na2HPO4
One mole of H+ will react with one mole of Na2HPO4 to given one mole of NaH2PO4
Na2HPO4 + H+ ---> NaH2PO4
Now this one mole formed NaH2PO4 will further react with 0.25 moles of H+ left to form 0.25 moles of H3PO4 and 0.75 moles of NaH2PO4 will remain in the solution
So this will result into formation of a buffer of phosphoric acid and NaH2PO4
NaH2PO4 + H+ ---> H3PO4
pKa of H3PO4 = 2.1
so pH = pKa + log [salt] / [acid] = 2.1 + log [0.75 / 0.25] = 2.58
so the pH will be in between 2.1 to 7.2