Introduction to Organic Chemistry
The field of chemistry which deals with the studies of reactions, structures, and properties of organic compounds that comprise carbon bonded through covalent bonding is organic chemistry. The studies regarding the structure of organic compounds could be determined with the help of structural formulas. In order to know about the behavior of organic compounds, a study on the properties has to be done. Both physical properties and chemical properties, the origin of chemical reactivity come under the study regarding the properties of organic compounds. The chemical preparation of polymers, drugs, natural products, and the study of separate organic molecules in the lab come under the study of organic reactions.
Vinyl Group
Vinyl group is the name given to the functional group of -CH=CH2. It can be seen as an ethene molecule with one less hydrogen in number. Hence it is also called as ethenyl group at times.
Straight Chain Hydrocarbons
The requirement to identify each compound needs a richer number of words than informative prefixes like n and iso. The identification of organic molecules is made easier by the use of systematic nomenclature schemes. The organic chemistry nomenclature has two types: traditional and systematic. Common names arise in many forms, but share the characteristic that a link through name and form is unnecessary. The name that matches a certain structure clearly must be remembered as knowing a person's name. In contrast, systemic names, including an overall common set of laws, are locked specifically to the chemical structure.
Unsaturated Hydrocarbon
Following are few examples of alkenes with their general molecular as well as their structural formulas:
Conjugated Compounds in Organic Chemistry
The delocalization of electrons in a molecule is called conjugation in organic chemistry. This delocalisation process of electrons leads to the shortenings or elongations of chemical bonds, but at the same time it causes changes in the chemical properties in conjugated molecules as compared to the non-conjugated ones. For example, conjugated molecules absorb light at longer wavelengths.
Alpha Carbon And Alpha Protons
The carbon directly attached to the functional group in an organic molecule is referred to as the alpha carbon and the hydrogen attached to an alpha carbon are termed as the alpha hydrogens or alpha protons. These alpha carbon atoms and alpha hydrogen atoms are of importance because they undergo certain characteristic reactions in organic chemistry.
![### Understanding Valence Orbitals in an sp Hybridized Carbon Atom
**Question 7:**
What valence orbitals (hybridized and/or nonhybridized) are available on an sp-hybridized carbon atom?
**Explanation:**
In an sp-hybridized carbon atom, hybridization involves the mixing of one s orbital and one p orbital from the valence shell to form two equivalent sp orbitals. This leaves two unhybridized p orbitals. The hybridization process can be summarized as follows:
1. **Hybridized Orbitals:**
- **2 sp Orbitals:** These orbitals are linear and are oriented 180 degrees apart, suitable for forming strong sigma bonds.
2. **Nonhybridized Orbitals:**
- **2 p Orbitals:** These orbitals remain unhybridized and are available for forming pi bonds.
This configuration is typical in molecules with triple bonds, such as acetylene, where the two sp orbitals are involved in sigma bonding, and the two p orbitals form pi bonds. Understanding these concepts is crucial for predicting the geometry and bonding properties of molecules containing carbon atoms.](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2F1b5d3972-c92b-4ea1-a6eb-b1828bd93066%2Fcf833d74-6883-4092-af04-c97c75c0c48f%2Foflli0h.png&w=3840&q=75)
![](/static/compass_v2/shared-icons/check-mark.png)
step 1) Introduction :
Carbon has to form 2 covalent bonds which results in , it is having 2 unpaired electrons in its electronic configuration .This is according to the valence bond theory.
Carbon has 4 unpaired electrons so to form 4 bonds the configuration of carbon exists as .
has 2s and 2p orbitals which fused to form four equal hybrid orbitals.
Trending now
This is a popular solution!
Step by step
Solved in 2 steps
![Blurred answer](/static/compass_v2/solution-images/blurred-answer.jpg)
![Chemistry](https://www.bartleby.com/isbn_cover_images/9781305957404/9781305957404_smallCoverImage.gif)
![Chemistry](https://www.bartleby.com/isbn_cover_images/9781259911156/9781259911156_smallCoverImage.gif)
![Principles of Instrumental Analysis](https://www.bartleby.com/isbn_cover_images/9781305577213/9781305577213_smallCoverImage.gif)
![Chemistry](https://www.bartleby.com/isbn_cover_images/9781305957404/9781305957404_smallCoverImage.gif)
![Chemistry](https://www.bartleby.com/isbn_cover_images/9781259911156/9781259911156_smallCoverImage.gif)
![Principles of Instrumental Analysis](https://www.bartleby.com/isbn_cover_images/9781305577213/9781305577213_smallCoverImage.gif)
![Organic Chemistry](https://www.bartleby.com/isbn_cover_images/9780078021558/9780078021558_smallCoverImage.gif)
![Chemistry: Principles and Reactions](https://www.bartleby.com/isbn_cover_images/9781305079373/9781305079373_smallCoverImage.gif)
![Elementary Principles of Chemical Processes, Bind…](https://www.bartleby.com/isbn_cover_images/9781118431221/9781118431221_smallCoverImage.gif)