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lara31 [8.8K]
2 years ago
10

This is the equation for the thermite reaction:

Biology
1 answer:
mylen [45]2 years ago
6 0

The charge of Fe in Fe₂O₃ is +3.

Let's consider the equation for the thermite reaction:

Fe₂O₃ + 2 Al ⇒ Al₂O₃ + 2 Fe

One of the reactants is ferric oxide, we can calculate the charge of Fe in Fe₂O₃ considering that:

  • The sum of the charges of the atoms is equal to the charge of the compound.
  • The charge of a neutral compound is 0.
  • The charge of O in oxides is -2.

The charge of Fe in Fe₂O₃ is:

2Fe+3O = 0\\2Fe+3(-2)= 0\\Fe=+3

The charge of Fe in Fe₂O₃ is +3.

Learn more: brainly.com/question/11938054

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Answer:

This is history not biology

Explanation:

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A boy picks up an earthworm and place it on a white tile. He observed that the earthworm has difficulty in moving forward.
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A number of tiny hair like bristlez are present on the lower surface pf an earthworm's body. These bristles help it to get a good grip on the surface of q ground.However these bristles donot provide good grip on plain glass tiles.

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3 years ago
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Why did the petri dish get warm when hydrogen peroxide and liver were combined?
maks197457 [2]

Answer: The bubbles will form due to the liberation of oxygen gas and white spots will develop on the liver.

Explanation:

The liver is a vital organ, its function is to metabolize the toxins into less harmful metabolites, that are excreted out of the body.

The catalase is one of the enzymes that participate in the metabolic activities of the liver. In the given condition, when hydrogen peroxide and liver were combined. The catalase enzyme breaks down the hydrogen peroxide into water and oxygen. In this reaction, the oxygen gas is liberated, in the form of bubbles and this reaction produces white colored foam which later leaves white spots on the liver.

7 0
3 years ago
You know that (1) both
adoni [48]

Complete question

  • It has to be E. coli because it is positive for gapA
  • It can't be Salmonella, because it is negative for the invA marker but still makes people sick
  • It has to be used because it is positive for the apeE marker

Answer:

<u>1. It can't be Salmonella, because it is negative for the invA marker but still makes people sick </u>

  • A combination of positive results from the multiplex PCR inva, apee and gapa is used to definitively identify Salmonella.  
  • Pathogenic, or disease causing Salmonella is definitely not present, as inva is required for it to be pathogenic. The test did not detect the inva sequence, thus it is truly negative for this particular pathogen.

<u>2. It has to be E. coli because it is positive for gapA </u>

  • E. coli may be present, as gapa was detected- a presumptive positive. However, this may need to be definitively determined through further methods of sample analysis, such as 2D-gel electrophoresis.
  • apee may belong to another type of bacteria present within the initial sample, or there may be sample contamination

Explanation:

Polymerase chain reactions, PCRs are a form of nucleic acid amplification testing NAAT that exploit the mechanism of transcription by using a thermostable DNA polymerase. These require a sample of genetic material such as RNA or DNA; specific regions of the gene sequence are targeted for replication by primers.  In the presence of these specific gene sequences, the primers make billions of copies of the sequences.

However, if these gene sequences are absent, the primers are not capable of identifying and amplifying the sequence. This reaction is highly specific. Positives obtained have a high chance of being true positives and negatives have a high chance of being true negatives .

Pathogens or infectious agents that are capable of causing disease i.e. making people sick. Both E. coli and Salmonella are genuses of enteric bacteria capable of causing disease via fecal contamination. Common symptoms include

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This test would include primers for the detection of each sequence: gapa, apee, inva. Salmonella's inva was not detected, thus it is not present.

Further steps may include a 2 D gel  electrophoresis- here an electrical current is utilized to separate bands of DNA within the sample. This should correspond with an expected DNA  size in base pairs or bp  for E.coli- this should be determined by running the sample in the gel with a positive control, containing genetic material for E coli, and a negative control, of purified water to determine contamination.

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4 years ago
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yulyashka [42]
We need the label and location of the image lol
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