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Concept explainers
Interpretation: The effects of chlorofluorocarbon compound substitutes should be identified.
Concept Introduction:
Atmosphere: The atmosphere is defined as air that is layer of gases which surrounds the earth due to gravity of earth.
The earth atmosphere consists of layers such as thermosphere, mesosphere, stratosphere and troposphere depending on the temperature and its composition.
Stratosphere:
It is found below the mesosphere layer in which the concentration of ozone and other gases are high. The increasing temperature for this layer with respect to increasing height is due to the presence of high concentration of ozone and other gases in it.
The increased temperature is due to the response of UV radiation from sun and hence ozone is formed due to this reaction and the use of ozone is that it prevents the UV radiation from the sun which is actually harmful.
Troposphere:
The layer is below stratosphere layer and it is closest to the earth surface. It is wholly composed of major air that is 80% of the total mass and almost all the water vapor.
It is the thinnest place which is responsible for all weather conditions since it contains almost all amounts of water vapor with it.
Chlorofluorocarbon (CFC): They are compounds that contain only carbon, fluorine and chlorine with it. They are gases can be easily liquefied, have little ability to react readily, are non-poisonous and do not catch fire easily.
CFC substitutes: They are compounds that replace the CFC in order to control the ill effects of CFC towards ozone depletion. The example of such substitutes is as follows,
To determine: The effects for substitutes of CFC in earth atmosphere should be explained.
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Chapter 21 Solutions
EBK CHEMISTRY: ATOMS FIRST
- Draw the a-anomer cyclized pyranose Haworth projection of the below hexose. Circle the anomeric carbons. Number the carbons on the Fischer and Haworth projections. Assign R and S for each chiral center. HO CHO -H HO -H H- -OH H -OH CH₂OH Draw the ẞ-anomer cyclized furanose Haworth projection for the below hexose. Circle the anomeric carbons. Number the carbons on the Fischer and Haworth projections. HO CHO -H H -OH HO -H H -OH CH₂OHarrow_forwardName the below disaccharide. Circle any hemiacetals. Identify the numbering of glycosidic linkage, and identify it as a or ẞ. OH HO HO OH HO HO HO OHarrow_forwardWhat are the monomers used to make the following polymers? F. а. b. с. d. Вецер хочому なarrow_forward
- 1. Propose a reasonable mechanism for the following transformation. I'm looking for curved mechanistic arrows and appropriate formal charges on intermediates. OMe MeO OMe Me2N NMe2 OTBS OH xylenes OMe 'OTBSarrow_forwardWhat is the polymer made from the following monomers? What type of polymerization is used for each? а. ОН H2N но b. ن -NH2 d. H₂N NH2 довarrow_forwardCondensation polymers are produced when monomers containing two different functional groups link together with the loss of a small molecule such as H2O. The difunctional monomer H2N(CH2)6COOH forms a condensation polymer. Draw the carbon-skeleton structure of the dimer that forms from this monomer.arrow_forward
- What is the structure of the monomer?arrow_forward→ BINDERIYA GANBO... BINDERIYA GANBO. AP Biology Notes Gamino acid chart - G... 36:22 司 10 ☐ Mark for Review Q 1 Hide 80 8 2 =HA O=A¯ = H₂O Acid HIO HBrO HCIO Question 10 of 35 ^ Σ DELL □ 3 % Λ & 6 7 * ∞ 8 do 5 $ 4 # m 3 ° ( 9 Highlights & Notes AXC Sign out Carrow_forwardWhich representation(s) show polymer structures that are likely to result in rigid, hard materials and those that are likely to result in flexible, stretchable, soft materials?arrow_forward
- 3. Enter the molecular weight of the product obtained from the Williamson Ether Synthesis? OH OH & OH excess CH3l Ag₂Oarrow_forwardPlease answer 1, 2 and 3 on the endarrow_forwardIn the box below, specify which of the given compounds are very soluble in polar aprotic solvents. You may select more than one compound. Choose one or more: NaCl NH4Cl CH3CH2CH2CH2CH2CN CH3CH2OH hexan-2-one NaOH CH3SCH3arrow_forward
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