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2 years ago

Please help me on this question I'm confusied on it

Chemistry

2 answers:

Fynjy0 [20]2 years ago

7 0

Find the average speed of the car and enter those numbers.

Korolek [52]2 years ago

3 0

Answer:

So you need to look for the average speed of each car, which would allow you to then enter the numbers.

Explanation:

Hope this helps! Have a great say! :)

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How many grams of sodium metal are needed to make 29.3 grams of sodium chloride? given the reaction: 2na + cl2 → 2nacl?

Bess [88]

2Na + Cl2 → 2NaCl
46 g. ➡️ 117 g
x. ➡️ 29.3 g
$x = \frac{46 \times 29.3}{117} \\ x = 11.5 \: g$

5 0

3 years ago

Read 2 more answers

Define saturated and unsaturated fats

saul85 [17]

Answer:

SATURATED: Saturated fat is a type of fat in which the fatty acid chains have all or predominantly single bonds.

UNSATURATED: Unsaturated fats are loosely packed. They tend to be liquid at room temperature.

There are two main types of unsaturated fat:

Monounsaturated

Polyunsaturated

8 0

2 years ago

The decomposition of nitryl chloride is described by the following chemical equation: 2NO2C1(g) → 2NO2 (g)-C12 (g) Suppose a two

Gnoma [55]

Answer:

Second reaction

NO2 + F -------> NO2F

Rate of reaction:

k1 [NO2] [F2]

Explanation:

NO2 + F2 -----> NO2F + F slow step1

NO2 + F -------> NO2F fast. Step 2

Since the first step is the slowest step, it is the rate determining step of the reaction

Hence:

rate = k1 [NO2] [F2]

6 0

3 years ago

PLEASE ANSWEER THIS HURRY HURRRRRRRRRYY

klemol [59]

The first one would be it

6 0

3 years ago

In your discussion consider a SN2 reaction mechanism concept. Propose a modification of experimental procedure that would improv

Hitman42 [59]

Answer:

Here's what I get

Explanation:

You may have done a Williamson synthesis of guaifenesin by reacting guaiacol with 3-chloropropane-1,2-diol.

A. Mechanism

Step 1

NaOH converts guaiacol into a phenoxide ion.

Step 2

The phenoxide acts as the nucleophile in an SN2 reaction to displace the Cl from the alkyl halide.

B. Improve the yield

You probably carried out the reaction in ethanol solution — a polar protic solvent.

You might try doing the reaction in a polar aprotic solvent— perhaps DMSO.

A polar aprotic solvent does not hydrogen bond to nucleophiles, so they become stronger.

C. Another method of ether synthesis —dehydration of alcohols

Sulfuric acid catalyzes the conversion of primary alcohols to ethers.

This is also a nucleophilic displacement reaction.

Protonation of the OH converts it into a better leaving group.

Attack by a second molecule of alcohol forms the protonated ether.

A molecule of water then removes the proton.

6 0

3 years ago