有机化学双语课件Chpt_1
有机化学英文原版ppt
Number of Covalent Bonds to an Atom Atoms with one, two, or three valence electrons form one, two, or three bonds Atoms with four or more valence electrons form as many bonds as they need electrons to fill the s and p levels of their valence shells to reach a stable octet
1.1 Atomic Structure
Structure of an atom
Positively charged nucleus (very dense, protons and neutrons) and smal (10-15 m) Negatively charged electrons are in a cloud (10-10 m) around nucleus Diameter is about 2 × 10-10 m (200 picometers (pm)) [the unit angstrom (Å) is 10-10 m = 100 pm]
1.5 The Nature of the Chemical Bond
Atoms form bonds because the compound that results is more stable than the separate atoms Ionic bonds in salts form as a result of electron transfers Organic compounds have covalent bonds from sharing electrons (G. N. Lewis, 1916) Lewis structures shown valence electrons of an atom as dots Hydrogen has one dot, representing its 1s electron Carbon has four dots (2s2 2p2) Stable molecule results at completed shell, octet (eight dots) for main-group atoms (two for hydrogen)
有机化学英文课件
+ C H 3 C H 2 -O -H + C H 3 C H 2 -O -H
SN 2
+ C H 3 C H 2 -O -C H 2 C H 3 + O -H
H
H
H
A new oxonium ion
11-11
Preparation of Ethers
Step 3: proton transfer to solvent completes the reaction
+
CH 3 CH 2 -O -CH 2 C H 3 + O -H
H
H
proton tran sf er
+ CH 3 CH 2 -O -CH 2 C H 3 + H O -H
H
11-12ቤተ መጻሕፍቲ ባይዱ
Preparation of Ethers
Acid-catalyzed addition of alcohols to alkenes
Acid-catalyzed dehydration of alcohols
• diethyl ether and several other ethers are made on an industrial scale this way
• a specific example of an SN2 reaction in which a poor leaving group (OH-) is converted to a better one (H2O)
CH 3 CH3C=CH2 + H
+ O CH3
H
CH3 C H 3 C+C H 3 +
有机化学双语课程.ppt
21-5 Interconversion of Acids and Derivatives by Nucleophilic Acyl Substitution
材厚重、价格太高,学生难以负担;
国内尚未影印正式出版的英文教材,版权问题。
有机化学双语教学教材选择与改编
中文教材:
英文教材:
章节编排归类划一。 $ 章节编排不拘形式。
饱和烃 不饱和烃 芳香烃
饱和烃 不饱和烃
醇、硫醇 醚、硫醚
芳香烃
烃类化合物 合并归类
醇和醚插入不饱和烃与芳香烃之间
有机化学双语教学教材选择与改编
双语教学铺垫了基础。
形势趋动,各级重视,条件具备,恰逢时机。
有机化学双语教学课程建设 大连理工大学有机化学双语教学概况 有机化学双语教学教材选择与改编 有机化学双语教学指导思想与教学方式 有机化学及实验双语教学课程立体化建设
大连理工大学有机化学双语教学概况
起始时间:1990年开始开设化工英语强化班,
中文教材:
英文教材:
章节编排归类划一。 $ 章节编排不拘形式。
红外光谱 紫外光谱 核磁共振谱 质谱
红外光谱
紫外光谱
质谱
核磁共振谱 共轭烯烃
四大谱学分在三章中出现章
结构的表征 合并归类
有机化学双语教学教材选择与改编
中文教材:
英文教材:
章节编排归类划一。 $ 章节编排不拘形式。源自命名 物理性质 制备 反应
命名 物理性质 制备 反应
命名 物理性质 反应 制备
有机化学课件1, INTRODUCTION
7
1.1 Concept Development of Organic Chemistry
1770, Organic and Inorganic, T. Bergman (Sweden) 1806, Organic Chemistry, J. Berzelius (柏则里)(Germany) 1828, Preparation of urea from ammonium cyanate (F. Wohler, Germany)
Conjugate base Conjugate acid
Ka=[HB][A:]/[HA][B]
2. The Lewis Definition
A Lewis acid is a substance that accepts an electron pair and a Lewis
base is a substance that donates an electron pair.
C l C l A l
C H 3 +O
C l C H 3 C l A l O
C l
C H 3
C l C H 3
Lewis Acid
Lewis base
24
Equilibrium favors reaction of the stronger acid and stronger base to give the weaker acid and weaker base
2
CHAPTER 1, INTRODUCTION
Organic Chemistry: Natural science, Life science, Medicine Materials science, Polymeric materials Fine chemicals, Chemical industry
有机化学英语课件
Table 1.4 Lewis Structures for Elements 1-18 of the Periodic Table IA H IIA IIIA IVA VA VIA VIIA VIIIA
Li
Na
. . .
Be
Mg
Al
. .
B
.. ..
C Si
.. . . ..
N P
O
. . .. . . . . ..
Pauling Scale: Fluorine: 4.0. All other elements are assigned values in relation to fluorine.
Within a Periodic Table: Electronegativity values increase from left to right and decrease from top to bottom within a group. Electronegativity values of a particular element depends not only on its position in the Periodic Table but also on its oxidation state.
Formal Charge: The charge on an atom in a molecule or polyatomic ion.
1. Write a correct Lewis structure for the molecule or ion. 2. Assign to each atom all its unshared (nonbonding) electrons and one half its shared (bonding) electrons. 3. Compare this number with the number of valence electrons in the neutral, unbonded atom.
有机化学ppt课件完整版
重排反应通常发生在含有不稳 定结构或官能团的化合物中, 需要加热或加入催化剂。在重 排过程中,分子的骨架结构可 能发生变化。
重排反应在有机合成中具有重 要的应用价值,可以用于合成 具有特定结构或官能团的有机 化合物。同时,重排反应也是 研究有机化合物结构和性质的 重要手段之一。
08
有机化学在生活中的应 用
定义
特点
加成反应在有机合成中具有重要的应用价值,可以用 于合成各种烯烃、醇、醛、酮等有机化合物。
应用
加成反应通常发生在分子中的不饱和键上,需要一定 的反应条件和催化剂。
消除反应
定义
消除反应是指有机化合物分子中 失去一个小分子(如水、卤化氢
等),形成不饱和键的反应。
种类
包括脱水消除、脱卤化氢消除、 热消除等。
反应。此外,醇还可以与酸反应生成酯,是重要的有机合成原料。
酚类化合物结构与性质
结构特点 酚类化合物的分子中含有苯环和羟基(-OH)官能团,通 式为Ar-OH,其中Ar为苯基或其衍生物。
物理性质 酚类化合物一般为无色或淡黄色的固体或液体,具有特殊 的气味和较强的毒性。酚的熔点和沸点较高,易溶于有机 溶剂。
化学性质
03
可发生加成、氧化、还原等反应,如与氢气加成生成醇,被弱
氧化剂氧化成酸。
酮类化合物结构与性质
结构特点
羰基(C=O)两侧连接烃基或芳基,无双键性质。
物理性质
沸点较高、难溶于水、易溶于有机溶剂。
化学性质
主要发生加成和还原反应,如与氢气加成生成醇,被还原剂还原 成仲醇。
醌类化合物结构与性质
结构特点
04
醇、酚、醚类化合物
醇类化合物结构与性质
01
结构特点
有机化学PPT课件
目录
• 有机化学简介 • 有机化学基础知识 • 有机化学反应 • 有机化学的应用 • 有机化学的未来发展
01 有机化学简介
有机化学的定义
总结词
有机化学是一门研究有机化合物 的组成、结构、性质、合成和反 应的学科。
详细描述
有机化学主要关注碳氢化合物及 其衍生物,即有机化合物,它们 是构成生命体的基本物质。
将有机化学与计算机科学、数学等学科交叉融合,利用计算机模拟和预测有机化学反应和 分子的性质,为有机化学研究和应用提供新的工具和手段。
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有机化学的发展历程
总结词
有机化学的发展经历了从天然有机化学到合成有机化学的演变,并不断推动着 人类社会的进步。
详细描述
早期的有机化学主要研究天然有机物,如动植物体内的化合物。随着科技的发 展,合成有机化学逐渐崛起,人们开始能够合成大量原本自然界不存在的有机 化合物,从而极大地丰富了人类的物质生活。
农业领域
1 2
农药合成
有机化学在农药合成中扮演着关键角色,通过设 计并合成新的农药分子,可以开发出更安全、更 有效的农药。
植物生长调节剂
有机化学也可用于合成植物生长调节剂,通过调 节植物生长代谢,提高作物产量和品质。
3
转基因作物
利用有机化学手段,可以修改作物的基因组,培 育出抗逆性更强、产量更高的转基因作物。
举例
乙醇被氧化生成乙醛。
04 有机化学的应用
医药领域
药物合成
有机化学在药物合成中发挥着重要作用,通过设计并合成新的有 机分子,可以开发出具有治疗作用的创新药物。
药物代谢
有机化学也涉及药物代谢的研究,了解药物在体内的代谢过程有助 于优化药物的疗效和降低副作用。
有机化学英文课件chapter1
M a c in to s h P IC T im a g e fo rm a t
is n o t s u p p o rte d
• we use a single-headed (barbed) curved arrow to show the transfer of one electron from Na to F
M a c in to s h P IC T im a g e fo r m a t
is n o t s u p p o r te d
3.0 - 2.1 = 0.9 • we show polarity by using the symbols d+ and d-, or by
using an arrow with the arrowhead pointing toward the negative end and a plus sign on the tail of the arrow at the positive end
• generally increases left to right in a row • generally increases bottom to top in a column
M a c in to s h P IC T im a g e fo rm a t
is n o t s u p p o rte d
to complete its valence shell; a chemical bond formed by sharing electrons is called a covalent bond • bonds may be partially ionic or partially covalent; these bonds are called polar covalent bonds
有机化学ppt课件完整版
有机化学ppt课件完整版目录•绪论•有机化合物的结构与性质•烃类化合物•烃的衍生物•有机合成与反应机理•生物活性有机化合物绪论碳氢化合物研究碳氢化合物(烃)的结构、性质、合成和反应机理。
碳氢化合物的衍生物研究烃的衍生物,如醇、醛、酮、羧酸、酯等有机化合物的结构、性质、合成和反应机理。
生命体系中的有机化合物研究生物体内的氨基酸、蛋白质、核酸、多糖等生命物质的结构、性质和功能。
经典时期19世纪初到20世纪初,以经验规律为指导,通过大量的实验总结出了许多有机化学的基本概念和原理。
萌芽时期从远古时期到18世纪,人们开始使用天然有机物,如木材、植物、动物等。
现代时期20世纪至今,以量子力学和统计力学为基础,发展出了现代有机化学的理论和方法,如分子轨道理论、价键理论、反应机理理论等。
环境领域有机化学在环境保护方面发挥着重要作用,如研究大气污染物、水体污染物的来源和治理方法等。
同时,有机化学也致力于开发环保材料和清洁能源。
材料领域合成纤维、塑料、橡胶等高分子材料广泛应用于服装、家居用品、交通工具等领域。
医药领域合成药物如抗生素、抗癌药物等对于治疗疾病具有重要意义。
同时,天然药物中提取的有效成分也是有机化学的研究对象。
农业领域合成农药和化肥对于提高农作物产量具有重要作用。
此外,生物农药和生物肥料的研发也需要有机化学的支持。
有机化学与生产生活的关系有机化合物的结构与性质碳原子通过四个共价键与其他原子或基团相连,形成复杂的有机分子结构。
碳原子的四价性键的极性空间构型碳原子与其他原子形成的共价键具有不同的极性,影响有机物的物理和化学性质。
有机化合物分子中的原子或基团在空间的排列方式不同,导致同分异构现象的产生。
030201有机化合物的结构特点03同分异构体的性质差异由于结构上的差异,同分异构体在物理性质、化学性质以及生物活性等方面表现出明显的不同。
01构造异构分子式相同但连接方式不同,如正丁烷和异丁烷。
02立体异构分子式相同、连接方式也相同,但空间构型不同,如顺反异构、对映异构等。
有机化学基础英文版
3
CH3
1
Is 5-(1’-methylethyl)-2,2,4-trimethyloctane
CH3 CH3
Is 4,5-diethyl-2,2-dimethylheptane
It is NOT 3,4-diethyl-6,6-dimethylheptane!
4
H3C
H2 C
2
CH OH
CH3
4
H3C
R C O R
I
Bromide
R C O NH2
Iodide
R C O Cl
Carboxylic acid
R C O O C O
Ester
R R C N
Ketone
H R N R O O
Amide
Acid Chloride
Anhydride
Imine
Nitro groupFra bibliotekA cyclic ester is called a lactone, a cyclic amide a lactam
The ‘substitution level’ of a carbon atom in an organic compound is determined by the number of attached hydrogen atoms:
tertiary carbon (one H)
H3C H2 C H3C C H2 CH3 CH CH CH CH3 H2 C C CH3 CH3 CH3
CH3 CH C H2 CH3
is 3-methyloctane, not 5-methyloctane
2'
H3C
major chain
有机化学 英文课件 chapter
9-14
Mechanism - SN1
9-15
Evidence of SN reactions
1. What is relationship between the rate of an SN reaction and:
• the structure of Nu? • the structure of RLv? • the structure of the leaving group? • the solvent?
M a c in to s h P IC T im a g e fo rm a t
is n o t s u p p o rte d
9-17
Kinetics
For an SN2 reaction,
• reaction occurs in one step • the reaction leading to the transition state involves the
haloalkane and the nucleophile • the result is a second-order reaction; first order in
haloalkane and first order in nucleophile
M a c in to s h P IC T im a g e fo rm a t
9-16
Kinetics
For an SN1 reaction
• reaction occurs in two steps • the reaction leading to formation transition state for
有机化学英文课件chapter2-71页PPT精选文档
M a c in to s h P IC T im a g e fo rm a t
is n o t s u p p o rte d
2-15
Nomenclature - IUPAC
• indicate the number of times the substituent appears by a prefix di-, tri-, tetra-, etc.
• use commas to separate position numbers
M a c in to s h P IC T im a g e fo rm a t
is n o t s u p p o rte d
2-13
Nomenclature - I UPAC
6. If there are two or more different substituents, • list them in alphabetical order • number from the end of the chain that gives the
u Structure and nomenclature
• to name, prefix the name of the corresponding openchain alkane with cyclo-, and name each substituent on the ring
• if only one substituent, no need to give it a number • if two substituents, number from the substituent of
《有机化学》英文教学课件:Chap 2 Cyclic hydrocarbon(2012)
C 109º28’
C
<109º28’
C >109º28’
A normal tetrahedron with a bond angle of 109º28’
A small ring will constrict this angle to less than 109º28’
A large ring will expand this angle to more than 109º28’
polycycli hydrocarbon
1
Section 1 Alicyclic hydrocarbon
Ⅰ. Classification and Nomenclature
These ring compounds are named by attaching the prefix “cyclo” to the name of the parent hydrocarbon.
Ring compounds will have angle strain if angle are forced to significantly smaller or larger than the ideal 109º28’.
6
bond angle
60° 90° 108° 120°
angle of deflexion
9
CH2 H2C 60º CH2
60º 109º28’.
( internuclear angle is 60º) ( interrobital angle is 109º28’ )
The internuclear angle (60º) and the interrobital angle (109º28’) are different for cyclopropane.
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•Wöhler’s Synthesis of Urea:
•Synthesis –Construct complex organic chemicals from simpler, more readily available ones (Chapter 8).
covalent bond is formed.
Ionic Bonds are based on the transfer of one or more
electrons from one atom to another. The resulting cation
and anion are electrostatically attracted to each other.
metal that of the preceding inert gas, the halogen that of
valence electrons:
Hydrogen can either lose an electron to form an H
an electron to form a H-, or hydride, ion:
configuration.
•In certain cases, one atoms supplies both of the electrons
in the bond:
•Often 4 electron (double) and 6 electron (triple) bonds are
formed:
•As a rule of thumb, electronegativity differences less
than 0.3 represent pure covalent bonds, from 0.3 to 2.0
polar covalent bonds, and greater than 2.0 ionic bonds.
•The separation of opposite charges in polar covalent
molecules results in the formation of dipoles:
Correct Lewis Structure Incorrect Lewis Structures
satisfy the octet rule:
½(# bonding electrons surrounding the atom)
In molecules such as nitric acid, charges occur on
individual atoms, even though the molecule itself is
neutral.
The 2 negative charges are delocalized over all three
Structures with a maximum of octets are most
Charges should be preferentially located on atoms with
electronegativity. If this conflicts with rule
1, then rule 1 takes precedence.
more important resonance contributors than those with
1 takes precedence over guideline 2:
If there are two or more charge separated resonance
structures which comply with the octet rule, the most
producing either constructive or destructive interference:
called s orbitals. The lowest energy s orbital is the 1s orbital.contains a spherical nodal surface.
Of slightly higher energy than the 2s orbital are 3 degenerate 2p orbitals. These orbitals are shaped like a figure 8 and point along the 3 Cartesian axes.
Aufbau principle assigns electrons to
Lower energy orbitals are filled before those with higher
No orbital may be occupied by more than two electrons. ( Exclusion Principle). If two electrons occupy a single orbital,
configuration.
The process of filling up the energy level diagram one electron at a time is called the Aufbau process.
The d orbitals on atoms of row 3 and higher are involved in the formation of expanded octets(10 and 12 electrons about
orbital places most of the electron probability to the left and right of
with the observed bond angle in the BeH2molecule.
Hybridization does not change the number of orbitals on
the atom. In this case two atomic orbitals are replaced by
two new hybrid orbitals. The two un-hybridized p orbitals
are still available to hold electrons.
approximately 109.5 approximately 120
The molecule, BH3is isoelectric with the methyl cation, CH3+.
Both involve sp2hybridization about the central atom.
contain lone pairs of electrons.
The bond angles in ammonia are 107.3o and that in water is
104.5o, both close to 109.5o. The slightly smaller bond
angles in ammonia and water are due to the slightly larger
volume requirements for lone pair electrons, which forces the
connectivity of atoms are called constitutional or structural
molecular structures.。