Synthetic fuels are usually:

Answers

Answer 1
Answer: liquid, gaseous, obtained from syngas, mixture of carbon monoxide and hydrogen

Related Questions

Name three major adaptations for life during the late Precambrian
During glycolysis, the steps between glucose and formation of the triose phosphates collectively a. consume two ATP and two NADH molecules b. produce two ATP and two NAD+ molecules c. consume two ATP molecules d. produce two ADP and two NADH molecules e. consume two NAD+ molecules
“Water covers 75 percent of Earth. 97 percent of water on Earth is salt water. Only 3 percent of water is available as fresh water, but most of this water is locked up in solid glaciers and polar ice caps.” Based on this information, which is the best approximation of the amount of water on the planet that is available for animals to drink?
How many atoms of nitrogen are in a chemical formula Ni(NO3)2?O 3O 2O 1O 6
What is the role of RNA?

Where do you find tundra?A. At high elevations
B. In Antarctica
C. North of the Arctic Circle
D. North of the Arctic Circle and at high elevations

Answers

The answer is D.North of the Arctic Circle and at high elevations

♡♡Hope I helped!!! :)♡♡

Not enough water in the leaf will decrease plant photosynthesis.
a. True
b. False

Answers

UR ANSWER IS A-TRUE 
HOPE IM RIGHT!!!!!!!!

Monohybrid Mice, i need help

Answers

Answer/Explanation:

  • See attached images showing the crosses on a Punnett square as well as the genotype and phenotypes of each cross.

I. Cross between a female Gg with a male gg (GG X gg):

1. Probability of getting gray offspring (Gg) = 2/4 (¼+ ¼) = ½  

2. Probability of getting albino offspring (gg) = 2/4 (¼+ ¼) = ½

3. There are 2 possible genotypes among the offspring, which are Gg and gg.

4. There are 2 possible phenotypes among the offspring, which are gray and albino coat color.

5. Probability of getting heterozygous offspring (i.e. Gg) = 2/4 = ½

6. Probability of getting homozygous offspring (i.e. GG or gg) = Probability of getting GG + Probability of getting gg = ½ + 0 = ½  

7. The color of the female that was crossed (i.e. Gg), is gray color. The allele for gray coat color (G) is dominant over the allele for albino coat color (g).

8. The color of the male (gg) that was crossed is albino. The recessive allele (g) for albino coat color, in its homozygous state would express itself in the absence of the dominant G allele for gray color.

II. Cross between homozygous gray female with a heterozygous male (GG X Gg):

1. Probability of getting gray offspring (GG or Gg) = 4/4 (i.e. ¼+ ¼ + ¼ + ¼ ) = 1  

2. Probability of getting albino offspring (gg) = 0  

3. There are only 2 possible genotypes among the offspring, which are GG and Gg.

4. There is only 1 possible phenotype among the offspring, which is gray coat color.

5. Probability of getting heterozygous offspring (i.e. Gg) = 2/4 (i.e. ¼+ ¼ ) = ½

6. Probability of getting homozygous offspring (i.e. GG or gg) = Probability of getting GG + Probability of getting gg = 0 + ½  = ½  

7. The genotype of the female that was crossed is GG, given that the female is homozygous gray.

8. The male crossed is a heterozygous male (Gg), the male is gray.

III. Cross between a gray female, whose father was albino, with a heterozygous male (Gg X Gg):

We can make a good guess of the genotype of the female, given that gray color is dominant over albino, and the father was albino (gg). The father can only contribute sperm having only (g) allele, while the mother must contribute only a (G) allele to give a gray offspring. The gray female is definitely heterogyzous female i.e Gg

1. Probability of getting gray offspring (Gg or GG) =  ¾ (½ + ¼)  

2. Probability of getting albino offspring (gg) = ¼

3. There are 3 possible genotypes among the offspring, which are GG, Gg, and gg.

4. There are 2 possible phenotypes among the offspring, which are gray and albino coat color.

5. Probability of getting heterozygous offspring (i.e. Gg) = 2/4 = ½  

6. Probability of getting homozygous offspring (i.e. GG or gg) = Probability of getting GG + Probability of getting gg = ¼ + ¼ = ½  

7. The genotype of the female is Gg. We know this because we were given that it is gray in color, and gray is dominant over albino. Also, given that the father was albino (gg), a (g) allele can only be contributed by the father to combine with the dominant (G) allele to give us a female that has heterozygous gray coat color (Gg).

8. The genotype of the male is Gg. We know this because we were given that it was a heterozygous male. If an organism is heterozygous, it has different alleles controlling that trait.

IV. Cross between an albino female, whose father was gray, with a gray male, whose mother was albino (gg X Gg):

The albino female’s genotype is gg, because the g allele is recessive. The gray male’s genotype, whose mother was albino (gg) is definitely Gg, because gray is dominant, and to get a gray offspring, a G allele from the mother of the male must combine with the g allele that the albino father can only contribute i.e. Gg or GG from mother X gg from father = Gg (the gray male offspring).

1. Probability of getting gray offspring =  ¼ + ¼ = ½  

2. Probability of getting albino offspring (gg) = ¼ + ¼ = ½  

3. There are 2 possible genotypes among the offspring, which are Gg, and gg.

4. There are 2 possible phenotypes among the offspring, which are gray and albino coat color.

5. Probability of getting heterozygous offspring (i.e. Gg) = ¼ + ¼  = ½  

6. Probability of getting homozygous offspring (i.e. gg or GG) = ½ + 0 = ½  

7. The genotype of the gray father of the albino female (gg) is Gg. Of the two possible genotypes of the gray father (i.e. GG or Gg), Gg is the most likely genotype to contribute the recessive g allele that would pair up with another g allele from the mother to give an albino female (gg), i.e. Gg (father) X Gg (Mother) or Gg (Father) X gg (Mother) = gg (albino female)

Final answer:

A monohybrid cross is a genetic cross that considers only one trait. Results from these crosses led to the concept of dominant and recessive traits and Mendel's Law of Segregation. Punnett squares visually present the likely outcomes of these crosses.

Explanation:

A monohybrid cross involves the mating of individuals who have two different alleles for a single trait. For example, Mendel ran several monohybrid crosses using pea plants. The trait being examined was the color of the pea—the parent plants had either green or yellow peas. After breeding a purebred yellow pea plant with a purebred green pea plant, all offspring were yellow, showing that yellow is the dominant trait and green the recessive.

Monohybrid crosses are useful tools in predicting the outcome of genetic crosses because they follow Mendel's Law of Segregation. According to this law, during the formation of reproductive cells, pairs of genetic traits separate, and offspring receive one factor from each parent.

A Punnett square is a tool that provides a visual representation of the possible combinations of genetic traits the offspring could inherit. For monohybrid crosses, a Punnett square will give a 3:1 ratio, representing the likelihood of the offspring expressing the dominant trait over the recessive trait, given that both parents are heterozygous.

Learn more about Monohybrid Cross here:

brainly.com/question/15314052

#SPJ11

What kind of evidence do scientists use in taxonomy

Answers

Scientist look at the homologous structures and the genetic similarities between the different organisms in taxonomy

Which type of tissue coats surfaces? a. connective tissue
b. epithelial tissue
c. muscle tissue
d. nervous tissue

Answers

Epithelial tissue coasts surfaces

If the DNA sequence 3’ GTTACAGCACAGGGTAAACTC 5’ is mutated to 3’ GTTACAGCACAGGGTAAACGC 5', what does it do to the protein produced?

Answers

Thats a long one, but I got you!

A change in the DNA sequence, such as the mutation you described from 3' GTTACAGCACAGGGTAAACTC 5' to 3' GTTACAGCACAGGGTAAACGC 5', can have a significant impact on the protein produced. This specific type of mutation is called a "point mutation" or "single-nucleotide mutation" because it involves the substitution of a single nucleotide (in this case, a C for a T).

The impact on the protein depends on the role of the altered DNA sequence in encoding the protein. Here are the possible outcomes:

1. **Silent Mutation:** If the mutation does not change the amino acid encoded by the affected codon (a triplet of three nucleotides), it's considered a silent mutation. In this case, the protein's structure and function remain unchanged, as the altered DNA sequence still codes for the same amino acid.

2. **Missense Mutation:** If the mutation changes the codon to one that encodes a different amino acid, it's called a missense mutation. This can lead to an altered protein with potentially different properties or functions, depending on the nature of the new amino acid.

3. **Nonsense Mutation:** If the mutation changes a codon to a stop codon (a codon that signals the end of protein synthesis), it leads to a truncated protein. The protein will be shorter than the original, possibly lacking critical functional domains.

4. **Frameshift Mutation:** In cases where insertions or deletions of nucleotides occur (shifting the reading frame), it can result in a frameshift mutation. This often leads to a nonfunctional or drastically altered protein.

To determine the specific impact of the mutation, you would need to translate the altered DNA sequence into its corresponding amino acid sequence and assess how the change affects the protein's function, structure, and properties. The type of mutation and its consequences can vary, and it's essential to consider the specific genetic code and the context within the protein-coding region.