Answer:
Wind between 39-46 mph can cause branches and limbs to break, make it hard for cars to stay on the road wind between 47-54 can cause lighting difficulties, wind between the 60-78 can cause trees to uproot and damage.
Explanation:
1. Always give your graph a title in the following form: "The dependence of (your dependent variable) on (your independent variable). <span><span>Let's say that you're doing a graph where you're studying the effect of temperature on the speed of a reaction. In this reaction, you're changing the temperature to known values, so the temperature is your independent variable. Because you don't know the speed of the reaction and speed depends on the temperature, the speed of the reaction is your dependent variable. As a result, the title of your graph will be "The dependence of reaction rate on temperature", or something like that.</span>
</span>2. The x-axis of a graph is always your independent variable and the y-axis is the dependent variable.<span>For the graph described above, temperature would be on the x-axis (the one on the bottom of the graph), and the reaction rate would be on the y-axis (the one on the side of the graph)
</span>3. Always label the x and y axes and give units.<span>Putting numbers on the x and y-axes is something that everybody always remembers to do (after all, how could you graph without showing the numbers?). However, people frequently forget to put a label on the axis that describes what those numbers are, and even more frequently forget to say what those units are. For example, if you're going to do a chart which uses temperature as the independent variable, you should write the word "temperature (degrees Celsius)" on that axis so people know what those numbers stand for. Otherwise, people won't know that you're talking about temperature, and even if they do, they might think you're talking about degrees Fahrenheit.
</span>4. Always make a line graph<span><span>Never, ever make a bar graph when doing science stuff. Bar graphs are good for subjects where you're trying to break down a topic (such as gross national product) into it's parts. When you're doing graphs in science, line graphs are way more handy, because they tell you how one thing changes under the influence of some other variable. </span>
</span><span>5. Never, EVER, connect the dots on your graph!Hey, if you're working with your little sister on one of those placemats at Denny's, you can connect the dots. When you're working in science, you never, ever connect the dots on a graph.Why? When you do an experiment, you always screw something up. Yeah, you. It's probably not a big mistake, and is frequently not something you have a lot of control over. However, when you do an experiment, many little things go wrong, and these little things add up. As a result, experimental data never makes a nice straight line. Instead, it makes a bunch of dots which kind of wiggle around a graph. This is normal, and will not affect your grade unless your teacher is a Nobel prize winner. However, you can't just pretend that your data is perfect, because it's not. Whenever you have the dots moving around a lot, we say that the data is noisy, because the thing you're looking for has a little bit of interference caused by normal experimental error.</span><span>To show that you're a clever young scientist, your best bet is to show that you KNOW your data is sometimes lousy. You do this by making a line (or curve) which seems to follow the data as well as possible, without actually connecting the dots. Doing this shows the trend that the data suggests, without depending too much on the noise. As long as your line (or curve) does a pretty good job of following the data, you should be A-OK.
</span>6. Make sure your data is graphed as large as possible in the space you've been given.<span><span>Let's face it, you don't like looking at little tiny graphs. Your teacher doesn't either. If you make large graphs, you'll find it's easier to see what you're doing, and your teacher will be lots happier.</span>
</span><span>So, those are the steps you need to follow if you're going to make a good graph in your chemistry class. I've included a couple of examples of good and bad graphs below so you know what these things are supposed to look like.</span>
Answer:
See the explanation
Explanation:
In this case, in order to get an <u>elimination reaction</u> we need to have a <u>strong base</u>. In this case, the base is the phenoxide ion produced the phenol (see figure 1).
Due to the resonance, we will have a more stable anion therefore we will have a less strong base because the negative charge is moving around the molecule (see figure 2).
Finally, the phenoxide will attack the <u>primary carbon</u> attached to the Cl. The C-Cl bond would be broken and the C-O would be produced <u>at the same time</u> to get a substitution (see figure 1).
the principal organic product formed by free-radical bromination of 2,2,4−trimethylpentane is 2-bromo-2,4,4-trimethylpentane.
what is free radical halogenation?
A substitution reaction in which a hydrogen atom is replaced with a halogen atom, via a free radical reaction mechanism. when this reaction is carrid out by bromine radical, it is called free radicle bromination. When bromine (
) treated with light (hν) it comes to homolytic cleavage of the Br-Br bond and give rise to bromine radicles.
free-radical bromination of 2,2,4−trimethylpentane
Bromination of an alkane includes the substitution of a bromine atom for a hydrogen atom. The following stages will be taken by 2,2,4-trimethylpentane during this reaction:
Initiation reaction: The production of a bromine free radical requires the initiation of heat or light.
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Propagation: This reaction relies heavily on hydrogen. This reaction is impossible if hydrogen is not present. Because tertiary free radicals are more stable than secondary and primary free radicals, they are favoured in this reaction.
Termination: The remaining free radical of bromide reacts with the tertiary free radical of 2,2,4-trimethylpentane to form 2-bromo-2,4,4-trimethylpentane.
the principal organic product formed by free-radical bromination of 2,2,4−trimethylpentane is 2-bromo-2,4,4-trimethylpentane.
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