A student sets up an experiment according to the table below. What question was the student most likely investigating?

1. A compound is found to contain

satela [25.4K]

Answer:

FeSO2

Explanation:

Please see attached picture for full solution.

8 0

3 years ago

Draw the product that valine forms when it reacts with excess CH3CH2OH and HCl followed by a wash with aqueous base.

-BARSIC- [3]

Answer:

Product: ethyl L-valinate

Explanation:

If we want to understand what it is the molecule produced we have to analyze the reagents. We have valine an amino acid, in this kind of compounds we have an amine group ( $NH_2$ ) and a carboxylic acid group ( $COOH$ ). Additionally, we have an alcohol ( $CH_3CH_2OH$ ) in the presence of HCl (a strong acid) in the first step, and a base ( $OH^-$ ).

When we have an acid and an alcohol in a vessel we will have an esterification reaction. In other words, an ester is produced. As the first step, the oxygen in the C=O (in the carboxylic acid group) would be protonated. In the second step, the ethanol attacks the carbon in the C=O of the carboxylic acid group producing a new bond between the oxygen in the ethanol and the carbon in the carboxylic acid. In step 3, a proton is transferred to produce a better leaving group ( $H_2O$ ). In step 4, a water molecule leaves the main structure to produce again the double bond C=O. Finally, a base ( $OH^-$ ) removes the hydrogen from the C=O bond to produce ethyl L-valinate

See figure 1

I hope it helps!

7 0

3 years ago

There can be many different colors of beetles within the same species.This is an example of

azamat

Answer:

natural selection

Explanation:

The process that results in changes to the genetic material of a population over time

6 0

2 years ago

Describe the particle mode of matter. what does the brownian motion tells us about the particles in matter?give other evidence t

svetlana [45]

Answer:

dium (a liquid or a gas). This pattern of motion typically consists of random fluctuations in a particle's position inside a fluid sub-domain, followed by a relocation to another sub-domain. Each relocation is followed by more fluctuations within the new closed volume. This pattern describes a fluid at thermal equilibrium, defined by a given temperature. Within such a fluid, there exists no preferential direction of flow (as in transport phenomena). More specifically, the fluid's overall linear and angular momenta remain null over time. The kinetic energies of the molecular Brownian motions, together with those of molecular rotations and vibrations, sum up to the caloric component of a fluid's internal energy (the Equipartition theorem).

Explanation:

3 0

2 years ago

In a two-step synthesis, C6H11Br is converted into C6H12O. From the structure of the product, molecular formula of the starting

tamaranim1 [39]

Answer:

See explanation below

Explanation:

The question is incomplete. However in picture 1, you have the starting materials and the structure of the product, which you miss in this part.

Now, in picture 2, you have the starting reactant and the product, and the mechanism that is taking place here.

First, all what we have here is an acid base reaction. In the first step, we are using the acid medium to convert the reactant into an alcohol. The bromine there, is not leaving the molecule yet, because it's neccesary for the next step. The starting reactant is an alkene, in that way, we can convert the reactant in the first step into a secondary alcohol. In other words, the first reaction is a alkene hydration.

In the second step, we use a strong base. You may say this is a strong nucleophile and will do a Sn2 reaction to form another alcohol there, but it's not the case, because, before any kind of reaction happens, the priority here is always the acid base, so the base will react with the acidic hydrogen. In this case, it will substract an hydrogen from the OH. When this happens, the lone pair will do an auto condensation here, and attacks the bromine in the molecule. In this way, the molecule will become a cyclomolecule, and that way it form the final product.

See picture 2, for mechanism

8 0

3 years ago