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ratelena [41]
3 years ago
8

4. Calculate the mass of each element:

Chemistry
1 answer:
olga2289 [7]3 years ago
5 0
A) 13g
b) 2.68g (2dp)
c) 51.87g

Tip: mass = moles x Mr
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Consider a reaction that has a positive ΔH and a positive ΔS. Which of the following statements is TRUE?A) This reaction will be
Alja [10]

Answer: A) This reaction will be spontaneous only at high temperatures

Explanation:

\Delta G= +ve, reaction is non spontaneous

\Delta G= -ve, reaction is spontaneous

\Delta G= 0, reaction is in equilibrium

Using Gibbs Helmholtz equation:

\Delta G=\Delta H-T\Delta S

Given : \Delta H=+ve

\Delta S=+ve

\Delta G=(+ve)-T(+ve)

\Delta G=(+ve)(-ve)

Thus the value of  \Delta G  is negative and spontaneous when temperature is high.

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3 years ago
1. Describe the process of gene splicing.
AnnyKZ [126]

Answer:

The DNA is cut using special chemicals called restriction enzymes,.

DNA ligase are used to insert genes and other pieces of DNA into plasmids.

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1 year ago
What are the benefits of taxes? What is the relationship between taxes and the government?
marin [14]

collect this money and use it to finance social projects

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3 0
2 years ago
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The Lucas test has _______ results based on the type of alcohol present because the reaction involves a _________, which is ____
Olin [163]

Answer:

1) positive

2) carbocation

3) most stable

4) faster

Explanation:

A common test for the presence of alcohols can be achieved using the Lucas reagent. Lucas reagent is a mixture of concentrated hydrochloric acid and zinc chloride.

The reaction of Lucas reagent reacts with alcohols leading to the formation of an alkyl chloride. Since the reaction proceeds via a carbocation mechanism, tertiary alcohols give an immediate reaction. Once a tertiary alcohol is mixed with Lucas reagent, the solution turns cloudy almost immediately indicating an instant positive reaction.

Secondary alcohols may turn cloudy within five minutes of mixing the solutions. Primary alcohols do not significantly react with Lucas reagent obviously because they do not form stable carbocations.

Therefore we can use the Lucas reagent to distinguish between primary, secondary and tertiary alcohols.

5 0
3 years ago
Alkenes can be converted to alcohols by reaction with mercuric acetate to form a ?-hydroxyalkylmercury(II) acetate compound, a r
Goshia [24]

Answer:

The simplified mechanism and products are on the picture.

Explanation:

If we have the symmetrical alkene the addition of mercury and OH group is not regioselective but when we have more donors for one of Carbons in alkene then the OH group will go there.

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3 years ago
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