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Y_Kistochka [10]
3 years ago
5

What are some sources of resistance? (Check all

Engineering
1 answer:
Zarrin [17]3 years ago
7 0

Answer:

All of them.

Explanation:

I take this class rn too and those are answers

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Explain the LWD process why is it important in drilling operations?
barxatty [35]

Answer:

Logging while drilling (LWD) is a technique of conveying well logging tools into the well borehole downhole as part of the bottom hole assembly (BHA). ... In these situations, the LWD measurement ensures that some measurement of the subsurface is captured in the event that wireline operations are not possible.

Explanation:

pls mark brainliest

6 0
2 years ago
Open the"stateData3.c" program and try to understand how the tokenization works. If you open the input file "stateData.txt", you
babymother [125]

Answer:

Kindly see explaination

Explanation:

Code

#include<stdio.h>

#include<stdlib.h>

#include<string.h>

#define size 200

int main(void)

{

int const numStates = 50;

char tempBuffer[size];

char tmp[size];

char fileName[] = "stateData.txt"; // Name of the text file (input file) which contains states and its populations

char outFile[] = "stateDataOutput1.txt"; // Output file name

// Open the input file, quit if it fails...

FILE *instream = fopen(fileName, "r");

/* Output File variable */

FILE *opstream;

if(instream == NULL) {

fprintf(stderr, "Unable to open file: %s\n", fileName);

exit(1);

}

//TODO: Open the output file in write ("w") mode

/* Opening output file in write mode */

opstream = fopen(outFile, "w");

//TODO: Read the file, line by line and write each line into the output file

//Reading data from file

while(fgets(tmp, size, instream) != NULL)

{

//Writing data to file

fputs(tmp, opstream);

}

// Close the input file

fclose(instream);

//TODO: Close the output file

/* Closing output file */

fclose(opstream);

return 0;

}

5 0
3 years ago
Can you solve this question​
Alecsey [184]

Answer:

eojcjksjsososisjsiisisiiaodbjspbcpjsphcpjajosjjs ahahhahahahahahahahahahahahahhhahahahaahahhahahahahaahahahahaha

6 0
3 years ago
Read 2 more answers
A large retirement village has a total retail employment of 120. All 1600 of the households in this village consist of two nonwo
polet [3.4K]

Answer:

See explaination

Explanation:

Please kindly check attachment for the step by step solution of the given problem.

5 0
3 years ago
How would you describe what would happen to methane if the primary bonds were to break?
erastova [34]

Answer:

All the bonds in methane (CH4CH4) are equivalent, and all have the same dissociation energy.

The product of the dissociation is methyl radical (CH3CH3). All the bonds in methyl radical are equivalent, and all have the same dissociation energy.

The product of that dissociation is methylene (CH2CH2). All the bonds in methylene are equivalent, and all have the same dissociation energy.

The product of that dissociation is methyne (CHCH) .

The C-H bonds in methane do not have the same dissociation energy as C-H bonds in methyl radical, which in turn do not have the same dissociation energy as the C-H bonds in methylene, which are again different from the C-H bond in methyne.

If (by some miracle) you were able to get all four bonds in methane to dissociate absolutely simultaneously, they would all show the same dissociation energy… but that energy, per bond broken, would be different than the energy required to break just one C-H bond in methane, because the products are different.

(In this case, it’s CH4→C+4HCH4→C+4H versus CH4→CH3+HCH4→CH3+H.)

To alter hydrocarbons you add enough energy to break a C-H bond. Why does only one bond break? What concentrates the energy on one C-H bond?

the weakest CH bond is the one that breaks. in plain alkanes it has to do with the molecular orbital interactions between neighboring carbon atoms. look at propane for example. the middle carbon has two C-C bonds, and each of those C-C bonds is strengthened by slight electron delocalization from the C-H bonds overlapping with the antibonding orbitals of the adjacent carbons.

since the C-H bonds on the middle carbon donate electron density to both of its neighbors, those two are weakest.

one of them will break preferentially.

which one actually breaks depends on the reaction conditions (kinetics). frankly it's whichever one ramdomly approaches a nucleophile first. when the nucleophile pulls of one of the H's, the other C-H bonds start to share (delocalize) the negative charge across the whole molecule. so while the middle C feels the majority of the negative charge character, the other two C's take on a fair amount as well...

by the way, alkanes don't really like to break and form anions like that.

a better example would be something like isopropyl iodide, where the C-I bond breaks and the I carries away the electron pair, forming a carbocation (also not particularly stable, but more so than the carbanion).

7 0
3 years ago
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