Answer: (Structure attached).
Explanation:
This type of reaction is an aromatic electrophilic substitution. The overall reaction is the replacement of a proton (H +) with an electrophile (E +) in the aromatic ring.
The aromatic ring in p-fluoroanisole has two sustituents, an <u>halogen</u> and a <u>methoxy group</u>, which are <em>ortho-para</em> directing substituents.
Aryl sulfonic acids are easily synthesized by an electrophilic substitution reaction aromatic using <u>sulfur trioxide as an electrophile</u> (very reactive).
The reaction occurs in three steps:
- The attack on the electrophile forms the sigma complex.
- The loss of a proton regenerates an aromatic ring.
- The sulfonate group can be protonated in the presence of a strong acid (H₂SO₄).
Normally, a mixture of <em>ortho-para</em> substituted products would be obtained. However, since both <em>para</em> positions are occupied, only the <em>ortho </em>substituted product is obtained here.
Nothing, he shouldn’t be able to move it. Think about it like this say you try really hard to push something that is 5,000 pounds and you push as hard as you can. Well you can’t move it bc it weighs more than you can push. I’m sure their is a equation you can use to see how much you can push (body weight=force?)
i guess its e) Mn (VII)
if it was wrong pls let me knw
Answer: 3 significant figures
Explanation: because in scientific notation only the before and after decimal number are considered but in standard form all numbers including exponents are all significant figures
<h2>
→
</h2>
Explanation:
Ethanol can be oxidized to ethanal or acetaldehyde which is further oxidized to acid that is acetic acid.
→ [oxidation by loss of hydrogen]
-
An oxidizing agent potassium dichromate(VI) solution is used to remove the hydrogen from the ethanol.
- An oxidizing agent used along with dilute sulphuric acid for acidification.
Acetaldehyde can also be reduced back to ethanol again by adding hydrogen to it by using a reducing agent that is sodium tetrahydro borate, NaBH4.
- The oxidation of aldehydes to carboxylic acids can be done by the two-step process.
- In the first step, one molecule of water is added in the presence of a catalyst that is acidic.
- There is a generation of a hydrate. (geminal 1,1-diol).
→ [reduction by the gain of electrons]
Here, the oxidizing agent used is in the presence of acetone.