Pre Nursing Student Dosage Calculation for Metoprolol: A Guide for Pre Nursing Students
In this video I will discuss calculating the dose of a drug from mg of drug into ml of a drug solution. A simple and easy method to get this calculation correct each and every time!
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All About the SN1 Mechanism - Lecture 29 has need for more editing
In this video I will discuss important topics from general chemistry that you should master before starting your journey in organic chemistry. Topics include: electronic structure or an atom, s orbitals, p orbitals, isotopes and electron configuration.
This video is part of my lecture series for Organic Chemistry One (1). Everything in this series is what I present to my students in Organic Chemistry.. If you are a student in organic chemistry be sure to take detailed notes and practice practice practice.
Good Luck and Good Chemistry!
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18
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Converting Grain Measurements to Milliliters of Morphine: A Comprehensive Guide
This video is for education only. Not to be used to dose patients. A doctor orders that you administer “Morphine grain 1/10”. The only available bottle of morphine is labeled “Morphine 10 mg/mL”. How many mL will you administer to the patient?
In this informative and educational YouTube video, we will be discussing the conversion of grains of morphine to milliliters of morphine. Morphine is a potent narcotic pain medication commonly used to manage severe pain. Incorrect dosing and administration can lead to serious consequences, including respiratory depression and even death. Therefore, it is crucial to understand the correct conversion from grains to milliliters to ensure accurate dosing.
The presenter starts by explaining the definition of a grain. A grain is a unit of mass used in the imperial and US customary systems, equal to approximately 64.8 milligrams. This unit is commonly used to measure the weight of small objects, such as medication. However, the metric system is used in the healthcare industry, where milligrams and milliliters are used to measure medication doses.
The presenter then moves on to explain the conversion process from grains to milliliters. To do this, the first step is to convert the grain measurement to milligrams.
Next, the presenter explains how to convert milligrams to milliliters. The conversion of milligrams to milliliters depends on the concentration of the medication, which is expressed as milligrams per milliliter (mg/mL). The concentration of the medication can be found on the label or by consulting a medication reference guide.
The presenter demonstrates this conversion using an example of morphine with a concentration of 10 mg/mL.
In conclusion, this YouTube video provides a clear and concise explanation of the conversion process from grains of morphine to milliliters of morphine. The video highlights the importance of accurate dosing and administration of medication to ensure patient safety. By following the guidelines provided in this video, healthcare providers can accurately convert medication doses and avoid potential errors.
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44
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Nursing School Math Problems: Milliters of Amoxicillin per Day to Total Milligrams of Amoxicillin
A patient with an uncomplicated lower respiratory infection is taking amoxicillin. On checking into the clinic, she shows you her medication: a bottle of pink liquid labeled "amoxicillin 120 mg/5 mL. The patient states she has taken four (4) 6.00 mLdoses in the past24 hours. What is the total amount of amoxicillin she has received in the past 24 hours?
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39
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Nursing School Math Problems: Liters per Hour (Liters/Hour) to drops per Minute (Drops/Minute)
In this video I will show you how to convert liters per hour (Liter/hour) to drops per minute (drops/minute).
Nursing school calculations made simple!! Nursing school calculations made easy!
Good Luck and Good Chemistry!
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How to Draw a Lewis Structure From a Molecular Formula C6H14O2 Help with Chemistry!
In this video I will show you a simple and effective method to draw a Lewis Structure from a complicated formula. Drawing Lewis Structures is an important skill to develop for any chemistry student. Watch this video for an easy way to draw Lewis Structures. I will show you some no fail strategies to draw Lewis Structures for an Organic Chemistry exam.
Good Luck and Good Chemistry!
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52
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How to Draw a Lewis Structure From a Molecular Formula C5H8Cl2 Help with Chemistry!
In this video I will show you a simple and effective method to draw a Lewis Structure from a complicated formula. Drawing Lewis Structures is an important skill to develop for any chemistry student. Watch this video for an easy way to draw Lewis Structures. I will show you some no fail strategies to draw Lewis Structures for an Organic Chemistry exam.
Good Luck and Good Chemistry!
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29
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Convert Meters to Feet Video Dimensional Analysis - 1 Minute Lesson (Made Extremely EASY!)
This video go over how to use dimensional analysis to convert meters (m) to feet (ft). This conversion is very common and very easy. Follow the instructions in this video and you will easily be able to convert meters to feet (feet to meters or meters to feet).
In your chemistry class (general chemistry, organic chemistry, nursing chemistry, prenursing, pre-nursing) you will be confronted with at least one unit conversion problem. Likely, you will encounter many unit conversion problems and unit conversion problems in disguise. In order to do any unit conversion problem, you will need to have an equality between the given and the needed unit. Equalities can be easily transformed into conversion factors. Indeed, on exams you will be able to solve unit conversion problems with ease.
Dimensional analysis (factor label method) the easy way to perform unit conversion problems. Indeed, it is important that you have a method to do unit conversions quickly, correctly and most importantly – easily! Dimensional analysis uses units to accomplish everything. In fact the units do all the work and you as the scientist only have to let them do the heavy lifting and you can be a pro at converting! First find in the question the given and needed units and the units do the rest.
Remember that in any conversion factor or equality the units are married to the numbers! For example:
3.2808 feet = 1 meter. The 3.2808 is ALWAYS with the feet and the 1 is ALWAYS with the meter!
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5
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Hydroboration Oxidation Reaction of Alkenes to Form Alcohols Help Me With Organic Chemistry!
The E2 reaction delivers alkene products. A reaction that follows an E2 mechanism becomes interesting when there are stereocenters that can deliver two diastereomers known as E or Z (cis or trans. The outcome of an E2 reaction is entirely predictable when you follow the rules. In this video I will show you how to use Newman projections to predict the E or Z cis or trans out come of these reactions. I will also show you how to do this without using a Newman Projection and get the same result!
The E2 mechanism is second order. This means that the base and the substrate exist together in the transition state of the rate determining step.
Failing organic chemistry? You do not have to fail Organic Chemistry!
This video is part of a series called How to be Successful in Organic Chemistry. In this series I go over numerous problems that a student could expect to see in there organic chemistry 1 course. Doing organic chemistry practice problems will make you more successful in organic chemistry and biochemistry.
I recommend that you download the problem from the link below and attempt the problem yourself and use this video to correct your work.
Download the problem from this video at the following link:
https://www.dropbox.com/s/is91t20u9rxjmqw/stereochemical%20outcome%20and%20the%20E2%20mechanism.key?dl=0
Good Luck and Good Chemistry!
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https://www.dropbox.com/s/oaj34qog1pkbpa3/Hydroboration%20Oxidation%20Reaction%20of%20Alkenes%20to%20Form%20Alcohols%20.pdf?dl=0
32
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The Oxymercuration-Demercuration of an Alkene to Form an Alcohol. Help Me With Organic Chemistry!
The E2 reaction delivers alkene products. A reaction that follows an E2 mechanism becomes interesting when there are stereocenters that can deliver two diastereomers known as E or Z (cis or trans. The outcome of an E2 reaction is entirely predictable when you follow the rules. In this video I will show you how to use Newman projections to predict the E or Z cis or trans out come of these reactions. I will also show you how to do this without using a Newman Projection and get the same result!
The E2 mechanism is second order. This means that the base and the substrate exist together in the transition state of the rate determining step.
Failing organic chemistry? You do not have to fail Organic Chemistry!
This video is part of a series called How to be Successful in Organic Chemistry. In this series I go over numerous problems that a student could expect to see in there organic chemistry 1 course. Doing organic chemistry practice problems will make you more successful in organic chemistry and biochemistry.
I recommend that you download the problem from the link below and attempt the problem yourself and use this video to correct your work.
Download the problem from this video at the following link:
https://www.dropbox.com/s/is91t20u9rxjmqw/stereochemical%20outcome%20and%20the%20E2%20mechanism.key?dl=0
Good Luck and Good Chemistry!
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https://www.dropbox.com/s/1q7rhe83ecyq1s4/The%20Oxymercuration-Demercuration%20of%20an%20Alkene%20to%20Form%20an%20Alcohol.pdf?dl=0
18
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Reaction of an Alkene With a Halogen and Water to Form a Halohydrin Help Me With Organic Chemistry!
The E2 reaction delivers alkene products. A reaction that follows an E2 mechanism becomes interesting when there are stereocenters that can deliver two diastereomers known as E or Z (cis or trans. The outcome of an E2 reaction is entirely predictable when you follow the rules. In this video I will show you how to use Newman projections to predict the E or Z cis or trans out come of these reactions. I will also show you how to do this without using a Newman Projection and get the same result!
The E2 mechanism is second order. This means that the base and the substrate exist together in the transition state of the rate determining step.
Failing organic chemistry? You do not have to fail Organic Chemistry!
This video is part of a series called How to be Successful in Organic Chemistry. In this series I go over numerous problems that a student could expect to see in there organic chemistry 1 course. Doing organic chemistry practice problems will make you more successful in organic chemistry and biochemistry.
I recommend that you download the problem from the link below and attempt the problem yourself and use this video to correct your work.
Download the problem from this video at the following link:
https://www.dropbox.com/s/is91t20u9rxjmqw/stereochemical%20outcome%20and%20the%20E2%20mechanism.key?dl=0
Good Luck and Good Chemistry!
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https://www.dropbox.com/s/0525y66hnc7ozh7/Reaction%20of%20an%20Alkene%20With%20a%20Halogen%20and%20Water%20to%20Form%20a%20Halohydrin%20%20.pdf?dl=0
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The Hydration of an Alkene to Form an Alcohol. Help Me With Organic Chemistry!
The E2 reaction delivers alkene products. A reaction that follows an E2 mechanism becomes interesting when there are stereocenters that can deliver two diastereomers known as E or Z (cis or trans. The outcome of an E2 reaction is entirely predictable when you follow the rules. In this video I will show you how to use Newman projections to predict the E or Z cis or trans out come of these reactions. I will also show you how to do this without using a Newman Projection and get the same result!
The E2 mechanism is second order. This means that the base and the substrate exist together in the transition state of the rate determining step.
Failing organic chemistry? You do not have to fail Organic Chemistry!
This video is part of a series called How to be Successful in Organic Chemistry. In this series I go over numerous problems that a student could expect to see in there organic chemistry 1 course. Doing organic chemistry practice problems will make you more successful in organic chemistry and biochemistry.
I recommend that you download the problem from the link below and attempt the problem yourself and use this video to correct your work.
Download the problem from this video at the following link:
https://www.dropbox.com/s/is91t20u9rxjmqw/stereochemical%20outcome%20and%20the%20E2%20mechanism.key?dl=0
Good Luck and Good Chemistry!
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https://www.dropbox.com/s/djggezihp7z0im3/The%20Hydration%20of%20an%20Alkene%20to%20Form%20an%20Alcohol.pdf?dl=0
16
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The Markovnikov Addition to an Alkene How to Apply Markovnikovs Rule
In this video I will demonstrate the Markovnikov addition of hydrogen bromide to an alkene.
Failing organic chemistry? You do not have to fail Organic Chemistry!
This video is part of a series called How to be Successful in Organic Chemistry. In this series I go over numerous problems that a student could expect to see in there organic chemistry 1 course. Doing organic chemistry practice problems will make you more successful in organic chemistry and biochemistry.
I recommend that you download the problem from the link below and attempt the problem yourself and use this video to correct your work.
Download the problem from this video at the following link:
https://www.dropbox.com/s/zcqi6ybfomvvo5s/The%20Markovnikov%20Addition%20to%20an%20Alkene%20How%20to%20Apply%20Markovnikovs%20Rul
Good Luck and Good Chemistry!
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e.pdf?dl=0
4
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Mechanism of the antiMarkovnikov's addition of HBr Using Hydrogen Peroxide Help Me With Organic Chem
In this video I will discuss the antiMarkovnikov Addition of bromine to an alkene. This mechanism uses preoxide to form bromide radicals that attack the alkene. In the case of an asymmetrical alkene the attack of the bromine radical can form a carbon free radical on the most substituted carbon or the least substituted carbon. From our knowledge of carbon free radical stability we know that forming a free radical on the most substituted carbon is the most stable. This means that the bromine free radical will attack the alkene in such a way as to form the most substituted carbon free radical.
The first step of this mechanism is the homolytic cleavage of the peroxide forming oxygen free radicals. The oxygen free radicals then attack hydrogen bromide. The oxygen free radical removes the hydrogen atom and produces the bromine free radical. The bromine free radical then attacks the least substituted carbon of the alkene resulting in the free radical forming on the most substituted carbon. The carbon free radical then attacks another molecule of hydrogen bromide, removing the hydrogen and forming another bromine free radical. This newly formed bromine free radical will attack another molecule of the alkene thus keeping the radical chain reaction going!
Failing organic chemistry? You do not have to fail Organic Chemistry!
This video is part of a series called How to be Successful in Organic Chemistry. In this series I go over numerous problems that a student could expect to see in there organic chemistry 1 course. Doing organic chemistry practice problems will make you more successful in organic chemistry and biochemistry.
I recommend that you download the problem from the link below and attempt the problem yourself and use this video to correct your work.
Download the problem from this video at the following link:
https://www.dropbox.com/s/is91t20u9rxjmqw/stereochemical%20outcome%20and%20the%20E2%20mechanism.key?dl=0
Good Luck and Good Chemistry!
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https://www.dropbox.com/s/lf44wsvidm99rvo/Mechanism%20of%20the%20antiMarkovnikov%27s%20addition%20of%20HBr%20Using%20Hydrogen%20Peroxide%20.pdf?dl=0
67
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Using Markovnikov's Rule to Predict the Product of the Acid Catalyzed Addition of Water to an Alkene
In this video I will discuss the mechanism and Markovnikov Addition of water to an alkene. This mechanism and video will illustrate Markovnikov's rule. In the first step of this mechanism the alkene acting as a base will hydronium and protonate it forming a carbocation. In the case of an asymmetrical alkene the carbocation could form on the most of the least substituted carbon. From our knowledge of carbocation stability we already know that the carbocation will form on the most substituted carbon. At the point water will attack the carbocation forming the protonated alcohol. Water will then deprotonate the alcohol reforming hydronium and creating the alcohol. This mechanism is acid catalyzed.
Failing organic chemistry? You do not have to fail Organic Chemistry!
This video is part of a series called How to be Successful in Organic Chemistry. In this series I go over numerous problems that a student could expect to see in there organic chemistry 1 course. Doing organic chemistry practice problems will make you more successful in organic chemistry and biochemistry.
I recommend that you download the problem from the link below and attempt the problem yourself and use this video to correct your work.
Download the problem from this video at the following link:
https://www.dropbox.com/s/is91t20u9rxjmqw/stereochemical%20outcome%20and%20the%20E2%20mechanism.key?dl=0
Good Luck and Good Chemistry!
Please subscribe to my channel by clicking the link below!
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https://www.dropbox.com/s/72yyzwe2ojldvm4/Using%20Markovnikov%27s%20Rule%20to%20Predict%20the%20Product%20of%20the%20Acid%20Canalized%20Addition%20of%20Water%20to%20an%20Alkene.pdf?dl=0
6
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