Identify the acids and the bases in the chemical equation.

Convert a pressure of 0.0248 mm Hg to the equivalent pressure in pascals (Pa). How did you get your answer ?

Rudik [331]

Hope this helps :) remember your conversions and just practice it's fairly easy:)

5 0

3 years ago

What is migrate? Help me pls

Juliette [100K]

Means moving from one place to the other

8 0

3 years ago

Read 2 more answers

What volume of 0.307 m naoh must be added to 200.0ml of 0.425m acetic acid (ka = 1.75 x 10-5 ) to produce a buffer of ph = 4.250

Blababa [14]

The buffer solution target has a pH value smaller than that of pKw (i.e., pH < 7.) The solution is therefore acidic. It contains significantly more protons $\text{H}^{+}$ than hydroxide ions $\text{OH}^{-}$ . The equilibrium equation shall thus contain protons rather than a combination of water and hydroxide ions as the reacting species.

Assuming that $x \; \text{L}$ of the 0.307 $\text{mol} \cdot \text{dm}^{-3}$ sodium hydroxide solution was added to the acetic acid. Based on previous reasoning, $x$ is sufficiently small that acetic acid was in excess, and no hydroxide ion has yet been produced in the solution. The solution would thus contain $0.2000 \times 0.425 - 0.307 \; x = 0.085 - 0.307 \; x$ moles of acetic acid and $0.307 \; x$ moles of acetate ions.

Let $\text{HAc}$ denotes an acetic acid molecule and $\text{Ac}^{-}$ denotes an acetate ion. The RICE table below resembles the hydrolysis equilibrium going on within the buffer solution.

$\begin{array}{lccccc}\text{R} & \text{HAc} & \leftrightharpoons & \text{H}^{+} & + & \text{Ac}^{-}\\\text{I} & 0.085 - 0.307 \; x& & 0 & & 0.307 \; x\\\end{array}$

The buffer shall have a pH of 4.250, meaning that it shall have an equilibrium proton concentration of $10^{4.250}\; \text{mol}\cdot \text{dm}^{-3}$ . There were no proton in the buffer solution before the hydrolysis of acetic acid. Therefore the table shall have an increase of $10^{-4.250}\;\text{mol}\cdot \text{dm}^{-3}$ in proton concentration in the third row. Atoms conserve. Thus the concentration increase of protons by $10^{-4.250}\;\text{mol}\cdot \text{dm}^{-3}$ would correspond to a decrease in acetic acid concentration and an increase in acetate ion concentration by the same amount. That is:

$\begin{array}{lcccccc}\text{R} & \text{HAc} & \leftrightharpoons & \text{H}^{+} & + & \text{Ac}^{-}\\\text{I} & 0.085 - 0.307 \; x& & 0 & & 0.307 \; x\\\text{C} & - 10^{-4.250} & & +10^{-4.250} & & +10^{-4.250} \\\text{E} & 0.085 - 10^{-4.250} - 0.307 \; x& & 10^{-4.250} & & 10^{-4.250} + 0.307 \; x\end{array}$

By definition:

$\text{K}_{a} = [\text{H}^{+}] \cdot [\text{Ac}^{-}] / [\text{HAc}]\\\phantom{\text{K}_{a}} = 10^{-4.250} \times (10^{-4.250} + 0.307 \; x) / (0.085 - 10^{-4.250} - 0.307 \; x)$

The question states that

$\text{K}_{a} = 1.75 \times 10^{-5}$

such that

$10^{-4.250} \times (10^{-4.250} + 0.307 \; x) / (0.085 - 10^{-4.250} - 0.307 \; x) = 1.75 \times 10^{-5}\\6.16 \times 10^{-5} \; x = 1.48 \times 10^{-6}\\x = 0.0241$

Thus it takes $0.0241 \; \text{L}$ of sodium hydroxide to produce this buffer solution.

6 0

3 years ago

Draw the structure(s) of the major organic product(s) of the following reaction. 1. lithium diisopropylamide / hexane 2. 1 eq. C

Jobisdone [24]

Answer:

See explanation below

Explanation:

You are not providing the starting material, however, I manage to find a similar question to this, so I'm gonna use it as a basis to help you answer yours.

Now let's analyze what is happening in the reaction so we can predict the final product.

We have a ketone here, reacting at first with LDA. This is a very strong base that is commonly used in reactions with ketones and aldehydes to promove a condensation. To do this, as LDA is a strong base it will occur firts an acid base reaction, substracting the most acidic hydrogen in the molecule (Which in this case, is the Beta hydrogen of the carbonile). This will cause an enolate formation.

Then, this enolate will react with the CH3I and form a new product. The final result would be a ketone with a methyl group now attached. In the picture 2, you have the mechanism and final product.

Hope this helps