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alisha [4.7K]
2 years ago
11

The western coast of the United States has been increasing in size for millions of years.

Chemistry
2 answers:
fredd [130]2 years ago
8 0

Answer:

accretion at convergent boundaries

Explanation:

gulaghasi [49]2 years ago
4 0
Accretion at convergent boundaries
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It depends on the pH level of the water.
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2 years ago
Read 2 more answers
NEED HELP ASAP WILL GIVE BRAINLYEST Organisms that are made up of prokaryotic cells are NOT ____________. Multicellular All of t
Serhud [2]

Explanation:

the answer is that prokaryotic cells are not multicellular

6 0
2 years ago
List four greenhouse gases in the atmosphere. For each gas, describe its prevalence in the atmosphere, its natural sources, its
lakkis [162]

Answer: Carbon Dioxide, Methane, Nitrous Oxide and Fuorinated Gases

Explanation:Carbon dioxide (CO2): Carbon dioxide enters the atmosphere through burning fossil fuels (coal, natural gas, and oil), solid waste, trees and other biological materials, and also as a result of certain chemical reactions (e.g., manufacture of cement). Carbon dioxide is removed from the atmosphere (or "sequestered") when it is absorbed by plants as part of the biological carbon cycle.

Methane (CH4): Methane is emitted during the production and transport of coal, natural gas, and oil. Methane emissions also result from livestock and other agricultural practices and by the decay of organic waste in municipal solid waste landfills.

Nitrous oxide (N2O): Nitrous oxide is emitted during agricultural and industrial activities, combustion of fossil fuels and solid waste, as well as during treatment of wastewater.

Fluorinated gases: Hydrofluorocarbons, perfluorocarbons, sulfur hexafluoride, and nitrogen trifluoride are synthetic, powerful greenhouse gases that are emitted from a variety of industrial processes. Fluorinated gases are sometimes used as substitutes for stratospheric ozone-depleting substances (e.g., chlorofluorocarbons, hydrochlorofluorocarbons, and halons). These gases are typically emitted in smaller quantities, but because they are potent greenhouse gases, they are sometimes referred to as High Global Warming Potential gases ("High GWP gases").

5 0
3 years ago
Why is only one diastereomer formed in this reaction? Relate your answer to the mechanism you drew. b) If you used cis-stilbene
crimeas [40]

Answer:

1. Diastereomers have different physical properties (unlike most aspects of enantiomers) and often different chemical reactivity. ... Many conformational isomers are diastereomers as well. Diastereoselectivity is the preference for the formation of one or more than one diastereomer over the other in an organic reaction.

2. The result is a trans dibromide, as shown in the equation below

Explanation:

Diastereomers (sometimes called diastereoisomers) are a type of a stereoisomer.[1] Diasteoreomers are defined as non-mirror image non-identical stereoisomers. Hence, they occur when two or more stereoisomers of a compound have different configurations at one or more (but not all) of the equivalent (related) stereocenters and are not mirror images of each other.[2] When two diastereoisomers differ from each other at only one stereocenter they are epimers. Each stereocenter gives rise to two different configurations and thus typically increases the number of stereoisomers by a factor of two.

2. the addition of bromine to the trans and

cis isomers of 1,2-diphenylethene, more commonly known as trans- and cis-stilbene.

H

H

H H

trans-stilbene cis-stilbene

m.p. 122-124°C b.p. 82-84°C

density 0.970 g/mL density 1.011 g/mL

M.W. 180.25 g/mol M.W. 180.25 g/mol

In both cases, the nucleophilic double bond undergoes an electrophilic addition reaction

by the bromine reagent which proceeds via a cyclic bromonium ion. The addition of

bromine begins at one side of the double bond (either side is equally likely, but only one

option is drawn) and is followed by attack of bromide ion on the bromonium ion (again,

attack could occur at either carbon since the ion is symmetric, but only one option is

drawn). The result is a trans dibromide, as shown in the equation below:

Since the cis and trans isomers of stilbene have different geometries, it follows

that upon reaction with bromine they give rise to stereoisomeric bromonium ions and,

eventually, products that differ only by their stereochemistry.

4 0
3 years ago
There are two steps in the usual industrial preparation of acrylic acid, the immediate precursor of several useful plastics. In
KIM [24]

Answer:

ΔH = -470.4kJ

Explanation:

It is possible to sum 2 or more reactions to obtain the ΔH of the reaction you want to study (Hess's law). Using the reactions:

1. CaC2(s) + 2H2O(l) → C2H2(g) + Ca(OH)2(s)ΔH = −414kJ

2. 6C2H2(g) + 3CO2(g) + 4H2O(g) → 5CH2CHCO2H(g)ΔH = 132kJ

6 times the reaction 1.

6CaC2(s) + 12H2O(l) → 6C2H2(g) + 6Ca(OH)2(s)ΔH = −414kJ*6 = -2484kJ

This reaction + 2:

6CaC2(s) + 3CO2(g) + 16H2O(l) →  + 6Ca(OH)2(s) + 5CH2CHCO2H(g) ΔH = -2484kJ + 132kJ = -2352kJ

As we want to calculate the net change enthalpy in the formation of just 1 mole of acrylic acid we need to divide this last reaction in 5:

6/5CaC2(s) + 3/5CO2(g) + 16/5H2O(l) →  + 6/5Ca(OH)2(s) + CH2CHCO2H(g) ΔH = -2352kJ / 5

<h3>ΔH = -470.4kJ</h3>

4 0
3 years ago
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