What have all living things evolved from?

Chemistry

2 answers:

GuDViN [60]3 years ago

6 0

Answer:

all living beings are involved from early spices

EastWind [94]3 years ago

3 0

Answer:

Coprolites.........!!!

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12. Chubchub runs a 440m lap in 1.2 minutes. How many laps will Chubchub

Svet_ta [14]

Answer:

the number of laps in the case when he run for 50 minutes is 18,333.33

Explanation:

The computation of the number of laps in the case when he run for 50 minutes is shown below:

Given that

He runs 440m lap in 1.2 minutes

So in 50 minutes he can have laps of

= 440 × 50 ÷ 1.2

= 18,333.33 laps

hence, the number of laps in the case when he run for 50 minutes is 18,333.33

3 0

3 years ago

Which of the following is one way that nuclear reactions differ from chemical<br> reactions?

Juliette [100K]

Answer:

Nuclear reaction takes place at the nucleus whereas chemical reaction involves valence electrons

Explanation:

6 0

4 years ago

Use the definition of molarity to calculate the concentration of 12.34 g of CaSO4 completely dissolved in water, with a solution

Ede4ka [16]

Answer:

[CaSO₄] = 36.26×10⁻² mol/L

Explanation:

Molarity (M) → mol/L → moles of solute in 1L of solution

Let's convert the volume from mL to L

250 mL . 1L/1000 mL = 0.250L

We need to determine the moles of solute. (mass / molar mass)

12.34 g / 136.13 g/mol = 0.0906 mol

M → 0.0906 mol / 0.250L = 36.26×10⁻² mol/L

8 0

3 years ago

Explain what a glycosolation reaction is

AVprozaik [17]

Answer:

The glycosylation reaction or glycoside formation is an organic reaction in which the hemiacetal group of cyclists ketoses or aldoses turns into acetals, named glycosides. Reaction in the attached picture.

Explanation:

Carbohydrates can be found in an open-chain form or a cyclic form. For the second one, the carbonyl group of the aldehyde could react with the alcohol group of the molecule to form the cycle. As shown in the attached picture, the alcohol group of this cyclic form could react with an alcohol (like methanol) in acidic conditions to form an acetal. These compounds are stable at neutral and acidic conditions, but they hydrolyze at basic conditions. This reaction produces both acetals anomers (α and β) because the attack of the nucleophile (alcohol) could be from both sides. However, the most stable anomer will predominate.