Orgo lab 2

Source of nitronium ion- nitric acid is not a sufficient electrophile alone.

So, if the temp is kept low, there will simply not be enough energy to reach this high activation energy and the polysubstituted prodcut will not form 3.

Their Rf values are smaller bc they are more Orgo lab 2 to the stationary, polar solid phase and dissolve less in the mobile phase and do not travel as far What are the major sources of experimental concern? Outcome with 6M HNO3? For example, let us say that my school refers to the second semester of organic chemistry lab as Advanced optical thermonuclear basket weaving.

The most straight forward way of doing that is seeing if the course your are planning to take is required for the Biology or Chemistry major at your school. If it was not mixed, the reactants would have acccumulated at the top, possibily leading to Orgo lab 2 Why is the flask warmed to 60 deg C after bromobenzene has been added?

To prevent excess heating, which would lead to polysubstitution What other measure is taken to ensure that polysubstitution does not occur? Just make sure you take the class. Pasteru Pipette is much longer than a regular pipette and prevents loss of material Why is the bromobenzene added dropwise to the acidic solution?

More importantly then the name is that you are in the proper course. Polysubstitution- once the bromobenzene reacts with one nitronium ion, it cant react with another.

Bromobenzene and nitric acid are insoluble as solvent in each other and the formation of bromonitrobenzene occurs at the interface of the two substances. Alone, nitric acid is not a strong enough electrophile to react with bromobenzene.

To ensure the rxn occured, the additional heat helps to overcome this deactivation Workup of products added to water? But with sulfuric acid, it is strong enough.

However, remember that "culturally" medicine, medical education, and medical school admissions committee are conservative ie adheres to traditional values, standards.

What is the overall rxn mechanism for this experiment? Without more nitric acid, the mixing might not be as successful and thus more unwanted byproducts.

TLC uses concept of partitioning btwn a polar solid phase and less polar mobile phase. The activation energy of the polysubstitution rxn is much higher bc nitrobromobenzene is more deactivated than bromobenzene. File this under "what goes around, comes around" some 20 or 30 years ago, freshman-general-introductory chemistry, and their associated labs, were typically called Qualitative Chemistry semester I and Quantitative semester II.

Separates any remaining bromobenzene, nitric and sulfuric acid into the water Workup of vacuum filtration?

Orgo Chem Lab 2- Electrophilic Aromatic Substitution Nitration of Bromobenzene

The reverse rxn can overheat and boil easily What is special about the apparatus set up for the nitration of bromobenzene? Para is not as soluble in ethanol. Bc the bulky substituents are in 1,4 positions symmetricalthe molecule is not polar, and thus is soluble in the nonpolar mobile phase on the TLC plate Equation?

As for the second semester organic requirement, there is recommendation by AAMC that second semester organic can be substituted by biochemistry. Para has the highest MP. Nitrobromobenzene is the only solid.

Our lab guy was obssessed with kitchen chemistry so 90 percent of our class mates became meth manufacturers. So if it was physics 3, you say so, or if it was ochemL 2, you say so.

Non-Student bad virus said: What other reagents could be used? The bromo group is an EWG and deactivates the benzene. Solvent- bromobenzene is not very soluble in the acidic solution so must be vigorously mixed 4.

This seems to have cause a flux and variation among the allopathic schools about if a second semester or organic lecture, second semester lab is required, recommended, etc.

But of course, follow the "Ronald Reagan" rule of "trust but verify. The reaction vessel cannot exceed 55 deg C Temperature control is achieved by… Cooling the rxn vessel, slowing the addition of bromobenzene, dropwise addition of bromobenzene Why did we continuously have to shake the flask? So following the "letter" of the requirements may not impress the committees who may want to see that classic two semester organic sequence.

Is this normal? (Orgo II Lab)

The nitration occurs at the surface of the bromobenzene and the acids. To thoroughly mix the contents. In contrast, para is nonpolar and therefore symmetrical and does not as easily dissolve in ethanol. Sulfuric acid is added to the nitric acid. To prevent this polysubstitution, the temp is kept below a certain mark.orgo lab 2 distillation Essay Organic Chemistry Sarah Perez Purpose The purpose of this lab is to demonstrate the separation of a two-component liquid mixture based upon their difference in boiling point.

Do you really have to take ORGO LAB before med school?

Jan 25,  · I have received two interviews for med school so far even though i havent taken orgo lab. Do you all think i definitely need to take it this semester?.

Start studying Orgo 2 lab exam 2. Learn vocabulary, terms, and more with flashcards, games, and other study tools. Orgo Lab 2 Report (4c) - Download as Word Doc .doc /.docx), PDF File .pdf), Text File .txt) or read online.

for organic chemistry. 1 CHEM Orgo I, S12, Exp 1 (Lab #2) (Molecular Models) PRELAB = IN-LAB WORKSHEET this week. 25 pts _____ Last Name, First Name (PRINT). Nov 03,  · A pre-med student conquers orgo, that most dreaded of courses, and discovers why the subject matters.

It’s more than knowing how to draw arrows.

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Orgo lab 2
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