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Nadya [2.5K]
2 years ago
6

50 POINTS for a legitimate response. Please answer the question, chose the correct unit conversions on the right. Please read th

rough the ENTIRE thing. Answer ASAP, please.

Chemistry
1 answer:
makkiz [27]2 years ago
5 0

Answer:

0.121 millimeters

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How mant low dose 81mg aspirin tablets can be made from 1.21 kg of aspirin​
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A ____________ alkene is more stable than a ____________ alkene because they have fewer steric interactions. In an elimination r
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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>

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Protozoa. A group of one celled organisms which live in water. Entamoeba histolytica is a protozoa, an amoeba which causes amoebic dysentery in man.

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