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Kobotan [32]
3 years ago
11

QUESTION:

Chemistry
2 answers:
Maurinko [17]3 years ago
4 0

Answer:

✔ Cumberland Gap

was a natural mountain pass through the Appalachian Mountains.

This is the Correct Answer!

This might not be the same Question. This is history 5th Unit.

brilliants [131]3 years ago
3 0

Answer:

C. A law passed by the British parliament that prohibited colonial movements west of the Appalachian Mountains.

Explanation:

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What is part of the muscular system?
Likurg_2 [28]

Answer:

skeletal, smooth, and cardiac muscles

Explanation:

Plz brainliest

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3 years ago
Pick the correct answer!
Leto [7]

Answer:

I think it would be b. The octet rule states that transition metal group elements tend to react so that they attain a noble gas electron configuration.

8 0
3 years ago
Determine if each of the following statements about chiral molecules is True or False and select the best answer from the dropdo
oee [108]

Answer:

See explanation

Explanation:

-)<u> True or False: All R stereocenters are dextrorotatory. </u>

The absolute configuration is based is in specific rules that are not related to the ability to deflect polarized light. <u>FALSE</u>

-)<u> True or False: Chiral centers in organic molecules will have 4 different groups attached to a carbon. </u>

<u />

A chiral carbon by definition is a carbon with 4 groups. <u>TRUE</u>

-)<u> True or False: A racemic mixture has an optical activity of 0. </u>

In a racemic mixture, we have equal amounts of enantiomers, and this cancels out the optical activity. <u>TRUE</u>

-)<u> True or False: Normal linear amines can be chiral centers. </u>

<u />

In primary amines, we have 2 hydrogens. Therefore all the groups can not be different. So, is <u>TRUE</u>

<u />

-)<u>True or False: Compound C has an optical activity of 0. </u>

<u />

We need to know the structure of the compound

<u />

-)<u>True or False: If the R isomer of a molecule has an optical rotation of + 25.7 degree then the S isomer of the molecule will have an optical rotation of -25.7 degree. </u>

<u />

If we have the exact opposite (as we have in this case) the magnitud of the optical activity value will remain and the sign will change. <u>TRUE</u>

-)<u>True or False: A CN is a higher priority than a CH2OH. </u>

<u />

In this case, a carbon is directly bonded to the chiral carbon. The carbon on CN is bonded to a nitrogen atom and the carbon on CH2OH is bonded to an oxygen. So, the CH2OH will have more priority because O has a higher atomic number. <u>FALSE</u>

<u />

-)<u>True or False: All molecules with chiral centers are optically active. </u>

<u />

We can have for example mesocompounds in which the optical activity is canceled out due to symmetry planes. <u>FALSE</u>

<u />

-)<u>True or False: To have an enantiomer a molecule must have at least two chiral centers. </u>

<u />

A pair of enantiomers is made between at least 1 chiral carbon. Enantiomer R and enantiomer S. <u>FALSE</u>

<u />

-)<u>True or False: Chiral molecules are always optically active. </u>

<u />

We can have racemic mixtures or mesocompounds with chiral carbons but without optical activity. <u>FALSE</u>

<u />

-)<u>True or False: A CH2CH2Br is higher priority than a CH2F. </u>

The "Br" atom is bonded in the third carbon (respect to the chiral carbon) and the "F" atom is bonded to the second carbon. Therefore CH2F has more priority than CH2CH2Br. <u>FALSE</u>

-)<u>True or False: Meso molecules with two stereocenters have a R,S configuration. </u>

<u />

On the compounds with R and S configuration at the same time can have symmetry planes so, we will not have optical activity. <u>TRUE</u>

<u />

<u>True or False: Diastereomers have the same physical properties except in a chiral environment. </u>

<u />

All diastereomers have the same physical properties. <u>TRUE</u>

<u />

<u>True or False: Compound H has an optical activity of 0. </u>

<u />

We have to have the structure of the compound.

<u />

<u>True or False: A C=C double bond is higher priority than a -CH(CH3)2.</u>

<u />

In the case of C=C, we can say that is equivalent to two carbon bonds without hydrogens. Therefore C=C has higher priority. <u>TRUE</u>

<u />

6 0
4 years ago
2KClO3 2KCl + 3O2
FinnZ [79.3K]
True, because most chemical reactions have more moles but not really.
Also that they decompose better. "not really"
4 0
3 years ago
Briefly describe how a potentiometric pHmeter works. (Hint: Describe how the pH meter measures the amount of H+ or OH- ions in a
KengaRu [80]

Answer:

Indicators show changes in the pH of a solution

Explanation:

A pH meter is an instrument that measures the hydrogen-ion activity in aqueous solutions, indicating the acidity or alkalinity of the solution expressed as pH .The pH meter measures the difference in electrical potential between a pH electrode and a reference electrode, hence the pH meter is sometimes referred to as a potentiometric pH meter. Potentiometric pH meters measure the voltage between two electrodes and display the result converted into the corresponding pH value. The instrument comprises of a simple electronic amplifier and a pair of electrodes, or alternatively a combination electrode, and some form of display calibrated in pH units. It usually has a glass electrode and a reference electrode, or a combination electrode. The electrodes, or probes, are inserted into the solution to be tested.

Organic indicators are chemical species that change their colour in response to changes in the pH of the solution. This implies that the anionic and protonated forms of the indicator possess different colours. Hence the colour changes in acidic, basic and neutral solutions. The images attached indicate the colour changes in phenolphthalein and methyl orange in acidic and basic media accordingly.

4 0
3 years ago
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