What kind of scientist would study how mistletoe harms trees?

Chemistry

1 answer:

posledela3 years ago

5 0

Answer:

Biologist

Explanation:

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Why is hydrogen placed with the elements in group 1a??

N76 [4]

Because it has atomic no. = 1 (according to modern periidic table)

5 0

3 years ago

The AE of a system that releases 12.4 J of heat and does 4.2 J of work on its surroundings It is_______ jA. 16.6 B. 12.4 C. 4.2

andre [41]

ANSWER

EXPLANATION

Given that

The energy released by the system is 12.4J

Work done on the surrounding is 4.2J

Follow the steps below to find the change in energy

In the given data, energy is said to be released to the surroundings

Recall, that exothermic reaction is a type of reaction in which heat is released to the surroundings. Hence, change in enthalpy is negative

Step 1; Write the formula for calculating change in energy

$\Delta E\text{ }=\text{ q }+\text{ w}$

Since heat is released to the surrounding, then q = -12J

Recall, that work done by the system on the surroundings is always negative

Hence, w = -4.2J

Step 2; Substitute the given data into the formula in step 1

$\begin{gathered} \text{ }\Delta E\text{ = q + w} \\ \text{ }\Delta E\text{ }=\text{ -12.4 }+\text{ \lparen-4.2\rparen} \\ \text{ }\Delta E\text{ = -12.4 - 4.2} \\ \text{ }\Delta E\text{ }=\text{ -16.6J} \end{gathered}$

Therefore, the change i

3 0

1 year ago

Compound A is an alkene that was treated with ozone to yield only (CH3CH2CH2)2C=O. Draw the major product that is expected when

DochEvi [55]

Answer:

2,2,3,3-tetrapropyloxirane

Explanation:

In this case, we have to know first the alkene that will react with the peroxyacid. So:

What do we know about the unknown alkene?

We know the product of the ozonolysis reaction (see figure 1). This reaction is an oxidative rupture reaction. Therefore, the double bond will be broken and we have to replace the carbons on each side of the double bond by oxygens. If $(CH_3CH_2CH_2)_2C=O$ is the only product we will have a symmetric molecule in this case 4,5-dipropyloct-4-ene.

What is the product with the peroxyacid?

This compound in the presence of alkenes will produce peroxides. Therefore we have to put a peroxide group in the carbons where the double bond was placed. So, we will have as product 2,2,3,3-tetrapropyloxirane. (see figure 2)