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kaheart [24]
3 years ago
15

This indicator becomes colored when the solution is no longer acidic.

Chemistry
1 answer:
Irina-Kira [14]3 years ago
3 0

Answer:

Is pink in base solution, it provides a visual signal that a solution has changed from acid to a base, is colorless in acid solution.

Explanation:

As all the indicator, phenolphtalein has the property that turns pink when the solution that you have reaches a value of a pH of 9 or above. From 0 to 8 in a pH scale, is colorless. This point in which an indicator changes is it called equivalence point.

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B. control rods and moderators

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Will mark as Brainliest.
SVETLANKA909090 [29]
<span>If I done the math correctly it is 3729J because you multiply 16.5 g  by the 2260 J/g and get 3729 J</span>
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4 years ago
What is the molar mass of CaCL2•2 H2O
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Answer:

147 amu

Explanation:

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6 0
3 years ago
A ____________ alkene is more stable than a ____________ alkene because they have fewer steric interactions. In an elimination r
Vesna [10]

Answer:

See explanation

Explanation:

A <u>trans</u> alkene is more stable than a <u>cis alkene</u> because they have fewer steric interactions.

<em>⇒ In a cis alkene there is steric hindrance, because the methyl groups are on the same side of the double bond. </em>

<em>Because of this steric crowding, there are van der Waals repulsive forces between the electron clouds of the groups. </em>

<em> </em>

<em>This decreases the stability of the cis alkene.</em>

<em />

In an elimination reaction, a geometry where the β hydrogen and the leaving group are on opposite sides of the molecule is called <u>anti</u> periplanar.

<em> ⇒ 'Anti’ refers to the two functional groups lying on opposite sides of the plane of the bond</em>

In an <u>SN1 </u>mechanism, a nucleophile attacks the carbocation, forming a substitution product,

<em> ⇒ The SN1 reaction is a substitution reaction, and means "nucleophilic substitution".The "1" says that the rate-determining step is unimolecular. Thus, the rate equation is often shown as having first-order dependence on electrophile and zero-order dependence on nucleophile.</em>

while in an <u>E1</u><u> </u>mechanism, a base removes a β hydrogen from the carbocation, forming a new π-bond.

<em> ⇒ E1 indicates a elimination, unimolecular reaction</em>

<em>This implies that the rate determining step of the mechanism depends on the decomposition of a single molecular species.</em>

<em>.This is a classic elimination reaction – forming a new C–C(π) bond, and breaking a C–H and C–leaving group bond.</em>

CH3CH2Br and NaOH react by an <u>SN2</u><u> </u>mechanism.

<em> ⇒  It's a type of reaction mechanism that is common in organic chemistry, where one bond is broken and one bond is formed, synchronously, (in one step.) </em>

Stronger bases, like hydroxide, favor<u> E2</u> reactions, whereas weaker bases, like water favor, <u>E1</u> reactions

Disubstituted alkenes always have the possibility to exist as two different <u>Diastereomer.</u>

<em>Diastereomer are stereoisomers that are not mirror images of one another and are non-superimposable on one another. They exist (always) in 2 forms.</em>

<u>Elimination reactions</u> are regioselective, favoring formation of the more substituted and more stable alkene.

6 0
3 years ago
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