None of the questions asked can be answered completely from the graph provided (GHG emissions: Direct, indirect and total Vs Year)
Reason:
1) Question A:<span>What caused a drop in GHG emissions around 2009?. This questions in pointing towards reason for drop of GHG emission around 2009. From the graph, it can be seen that there is a drop in GHG emission around 2009. However, information for reason for this drop is not available in graph.
2) Question B: </span>Did GHG emissions cause the melting of Arctic glaciers?. As mentioned earlier, the graph plotted provides information of GHG emissions: Vs Year. Information related to impact of GHG on environment is not available in graph.
3) Question C: <span>How much methane was emitted by homes between 1990 and 2000?. Graph provides information of direct and indirect emission for GHG. However, it lacks information about emission from residential or industrial sources.
4) </span>Question D: <span>Does industrial equipment release gases other than greenhouse gases?: Present study doesnot cover type of gases emitted from industrial equipment.
5) </span>Question E: <span>Which types of industries were included in the study?: Present graph has not specific information related to industries. </span>
Answer:
Glucose
Explanation:
Plants make glucose to store as energy.
Answer:
Percent error = 1.5%
Explanation:
Given data:
Measured value of density of graphite = 2.3 g/cm³
Percent error = ?
Solution:
Formula:
Percent error = [Measured value - Actual value / actual value] × 100
Actual/accepted value of density of graphite = 2.266 g/cm³
Now we will put the values:
Percent error = [2.3 g/cm³ - 2.266 g/cm³ / 2.266 g/cm³] × 100
Percent error = [0.034 g/cm³ / 2.266 g/cm³] × 100
Percent error = 0.015 × 100
Percent error = 1.5%
1.00*10^3
You’d need to lower the exponent because rounding to 3 sig figs changes the 9’s to - 1000. Keep the 0’s.
Explanation:
Dehydrohalogenation reactions occurs as elimination reactions through the following mechanism:
Step 1: A strong base(usually KOH) removes a slightly acidic hydrogen proton from the alkyl halide.
Step 2: The electrons from the broken hydrogen‐carbon bond are attracted toward the slightly positive carbon (carbocation) atom attached to the chlorine atom. As these electrons approach the second carbon, the halogen atom breaks free.
However, elimination will be slower in the exit of Hydrogen atom at the C2 and C3 because of the steric hindrance by the methyl group.
Elimination of the hydrogen from the methyl group is easier.
Thus, the major product will A
