Please someone who knows organic chemistry help me$.$ I have a question from a lab experiment in organic chemistry. Im going to give you information about the lab experiment. In this lab assignment, we will look in more detail at how easily alcohols, aldehydes and ketones leave

oxidize. The task must also shed light on how to detect and distinguish between carbonyl

the compounds, aldehyde and ketone. Part A: Oxidation of alcohols

Background:

During the oxidation of alcohols, different products are formed depending on whether the alcohol is primary,

secondary or tertiary. Primary alcohols are easily oxidized to aldehydes. Aldehydes allow

however, easily oxidize to carboxylic acids, so that the oxidation product from a primary alcohol is most often

the corresponding carboxylic acid. Secondary alcohols are also easily oxidized. A common one

oxidizing agent is sodium dichromate $($Na$2$Cr$2$O$7).$ The product will then be a ketone, which is difficult

can be oxidized further. Tertiary alcohols are generally not oxidizable. Weigh the octanol directly into a $100$ mL round bottom flask.

The oxidizing agent is prepared by mixing $5\mathrm{.}00$ g KMnO$4$ and $7\mathrm{.}90$ CuSO$45$ H$2$O in

a mortar and pestle to make the mixture homogeneous.

Weigh $12\mathrm{.}64$ g of the oxidizing agent into a glass weighing vessel and transfer to the round bottom flask.

The resulting reaction mixture is stirred vigorously with a spatula for one minute.

Mount a reflux condenser on the round flask and place the apparatus in a water bath of approx.

$100\backslash$deg C$.$ Turn on the cooling water.

After $1$ hour, the reaction is complete and the reaction mixture is cooled to room temperature.

In the round bottom flask, a solid by$-$product is formed and the desired oxidized product must

is desorbed from this. This is done by rinsing the contents of the flask well with hexane and then

pour the hexane into a beaker. This is done five times with $10$ mL of hexane each

time. The solid by$-$product can be chopped up with a spatula while rinsing to get out

as much product as possible.

The combined hexane fractions are filtered on a sinter funnel with suction, the filtrate is dried with

MgSO$4$ in an Erlenmeyer flask and filter into a $50$ mL round bottom flask and the solvent

is evaporated on the Rota Vapor in two rounds.

Distill the residue in a Hickman column at atmospheric pressure. Increase the heat slowly

the solution begins to evaporate $($not above step $8$ on heating mantle$).$ Transfer it

distilled the product with a pipette into a test tube $($of known weight$).$ Weigh the product and

calculate the dividend.

Examine whether the product is the desired product using gas chromatography $($GC$)$

For the GC analysis, mix $5\backslash$mu l of the product with approx. $15$ ml of diethyl ether.

The GC chromatogram and the IR spectrum must be delivered together with the report and the product

handed in on a marked sample glass and approved by the supervisor. My question is can you draw $,$ the essay for the oxidation of secondary alcohol and write what the individual parts are. If u can see the picture i inserted, its just an example of another. But it is just to show you what i mean. But remember to include with what the individual parts are called as well please.. Also please include the mechanism. And write the reaction equation. Thank you so much.