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FromTheMoon [43]
3 years ago
10

What is the product in the following reaction?

Chemistry
2 answers:
gizmo_the_mogwai [7]3 years ago
8 0
The products would be an alcohol and a salt. so it would be A.
castortr0y [4]3 years ago
7 0
Your answer would be a
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icang [17]
Your answer to that question is Fand N
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Classify the reaction that makes a firefly glow in terms of energy input and output
user100 [1]
It glow, so light energy go out of the system, exotermic
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What will be the product when zinc snd silver nitrate undergo a single-replacement reaction
daser333 [38]
<span>zinc, nitrate and silver.

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8 0
4 years ago
In a DNA sample, 15% of the bases are thymine (T). What percentage of the bases in this sample are cytosine (C)?
allochka39001 [22]

Answer:

C) 35%

Explanation:

Thymine pairs with adenine. If thymine is 15% then so would adenine be 15%. That leaves the reaminder to be 70%. Cytosine pairs with guanine, thereby, they would each be 35%.

3 0
3 years ago
Predict which member of each pair will be more acidic. Explain your answers. (a) methanol or tert-butyl alcohol (b) 2-chloroprop
Art [367]

Answer:

A. Methanol

B. 2-chloropropan-1-ol

C. 2,2-dichloroethanol

D. 2,2-difluoropropan-1-ol

Explanation:

Primary alcohols are stronger acids than secondary alcohols which are stronger than tertiary alcohols.

This trend is so because of the stability of the alkoxide ion formed(stabilising the base, increases the acidity). A more stabilised alkoxide ion is a weaker conjugate base (dissociation of an acid in water).

By electronic factors, When there are alkyl groups donating electrons, the density of electrons on th O- will increase a d thereby make it less stable.

By stearic factors, More alkyl group bonded to the -OH would mean the bulkier the alkoxide ion which would be harder to stabilise.

Down the group of the periodic table, basicity (metallic character) decreases as we go from F– to Cl– to Br– to I– because that negative charge is being spread out over a larger volume that is electronegativity decreases down the group.

Electronegative atoms give rise to inductive effect and a decrease in indutive effects leads to a decrease in acidity. Therefore an Increasing distance from the -OH group lsads to a decrease in acidity.

From above,

A. Methanol

B. 2-chloropropan-1-ol

C. 2,2-dichloroethanol

D. 2,2-difluoropropan-1-ol

6 0
4 years ago
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