(pending/10pts) 4. Draw the 1H-NMR for the reduction compound below. Label each peak on the NMR. You do not need to show integration. G B D FH A CE 5 4 3 2 1 0
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- After the reduction of camphor with NaBH4 experiment, you took a 1H-NMR of your product sample. The sample ave the following 1H-NMR singlas with the given integrations (2.314 and 9.497). Determine the product ratio of isoboreneol to borneol in this particular mixture.ORGO II NMR please help fill out the chart and label. my unknown is C6H10O.Can someone explain how to do an NMR Spec like this, better refurred to it as Spectroscopy unknown. I got a pop up that said this might be graded.... I legit got it off of a practice website and I can send the link here: https://www.nmr.tips/indexe.html if you guys really need to know (Sadly you have to pay to get the solutions and I already have a subscription here.)
- How to get the wt. sample, g.please provide the machanisms of 1a, 1e, 1fI got confused with the steps provided. In m= it should have an exponent raised to (-10) but during Step 2, the exponent (-10) in m is omitted. Second, I do not know the basis of the formula used in Step 2. Please provide a better explanation of the solution. Thank you.
- 1.) Which solutions should you have used to make your Beer's Law Plot? 2.) What property of the product of your reaction allowed you to use visible spectroscopy to analyze your results? 3.) Using your absorbance value from Equilibrium mixture 5 (E5), show your calculation for the concentration of FeSCN^2+ in sample E5. (Provided picture for the resources)If 16.7 mg of sunscreen dissolved in 25 mL of 2-propanol. After this diluted this stock solution by a factor of 10 and measured the UV-Vis absorption of this diluted sample as 0.54. What is the absorbance/mg of the sunscreen used? Good hand written explanation asapi need help with predicting the Ir spec for the final product i also need to make it look like the example with the table and the 1h-nmr digram i made an example of how it needs to look like the lab called Electrophilic Aromatic Substitution: Friedel-CraftsAlkylation